Copies to:
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Stephen Randall Titan Medical Inc. 170 University Avenue, Suite 1000 Toronto, Ontario M5H 3B3 Canada Tel: (416) 548-7522 |
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Richard Raymer James Guttman
Dorsey & Whitney LLP TD Canada Trust Tower Brookfield Place, 161 Bay Street, Suite 4310
Toronto, Ontario M5J 2S1 Canada
Tel: (416) 367-7376 |
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Manoj Pundit Borden Ladner Gervais LLP Bay Adelaide Centre, East Tower 22 Adelaide St W Toronto, Ontario M5H 4E3 Canada
Tel: (416) 367-6577 |
A.
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□
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upon filing with the Commission pursuant to Rule 467(a) (if in connection with an offering being made contemporaneously in the United States and Canada).
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B.
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ý
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at some future date (check the appropriate box below):
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1.
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□
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pursuant to Rule 467(b) on ( ) at ( ) (designate a time not sooner than 7 calendar days after filing).
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2.
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□
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pursuant to Rule 467(b) on ( ) at ( ) (designate a time 7 calendar days or sooner after filing) because the securities regulatory authority in the review jurisdiction has issued a receipt or notification of clearance
on ( ).
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3.
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□
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pursuant to Rule 467(b) as soon as practicable after notification of the Commission by the Registrant or the Canadian securities regulatory authority of the review jurisdiction that a receipt or notification of clearance has been issued
with respect hereto.
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4.
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ý
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after the filing of the next amendment to this Form (if preliminary material is being filed).
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Title of Each Class of Securities
to be Registered |
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Proposed Maximum
Aggregate Offering Price(1) |
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Amount of
Registration Fee(2) |
Units, each unit consisting of one Common Share and a Warrant to purchase a Common Share at $[•] per Common Share
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Common Share included as part of the Unit(3)(4)
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Warrant included as part of the Unit(3)(4)
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Common Shares underlying Warrant(3)
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Over-Allotment Units
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Common Shares included as part of the Over-Allotment Unit(3)(4)
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Over-Allotment Warrants included as part of the Over-Allotment Unit
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Common Shares underlying Over-Allotment Warrant(3)
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Broker Warrants(3)(4)
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Common Shares underlying Broker Warrants(3)
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Total
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$
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22,000,000
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$
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2,666.40
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New Issue
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September 23, 2019
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Price: US $[●] per Unit
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Price to the Public
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Agent’s Commission(1)
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Net Proceeds to the Company(2)
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Per Unit(3)…………....……….
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US $[●]
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US $[●]
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US $[●]
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Minimum Offering(4)...………..
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US $[●]
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US $[●]
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US $[●]
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Maximum Offering(4)……….....
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US $[●]
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US $[●]
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US $[●]
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(1)
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The Company has agreed to pay the Agent, on each Closing Date, a commission (the “Agent’s Commission”) equal to 7% of the aggregate gross proceeds of the Offering
(or US $[●] per Unit) including any proceeds raised through the sale of Over-Allotment Units (as defined herein) and/or Over-Allotment Warrants pursuant to the exercise of the Over-Allotment Option (as defined herein). In addition to the
Agent’s Commission, the Company will issue to the Agent, on each Closing Date, compensation warrants (“Broker Warrants”) to purchase such number of Common Shares (the “Broker Warrant Shares”) as is equal to 7% of the aggregate number of
Units and Over-Allotment Units issued pursuant to the Offering on such Closing Date. Each Broker Warrant, whether issued on the first Closing Date or on a subsequent Closing Date, shall entitle the Agent to acquire one Broker Warrant Share
at an exercise price equal to the Offering Price, subject to adjustment, for a period of 24 months following the first Closing Date. See “Plan of Distribution”. This short form prospectus also
qualifies the distribution of the Broker Warrants.
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(2)
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After deducting the Agent’s Commission, but before deducting expenses of the Offering (including listing fees) estimated to be approximately US $[●] in the event
of the Minimum Offering, and US $[●] in the event of the Maximum Offering, which will be paid from the gross proceeds of the Offering.
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(3)
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From the Offering Price, the Company will allocate US $[●] to each Offered Share and US $[●] to each Warrant.
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(4)
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Assuming no exercise of the Over-Allotment Option.
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(5)
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The Company has granted the Agent an option (the “Over-Allotment Option”), exercisable in whole or in part at any time and from time to time on the first Closing
Date or for a period of 30 days following the first Closing Date, to offer for sale such number of additional Units (the “Over–Allotment Units”) and/or Warrants (the “Over-Allotment Warrants”) as is equal to 15% of the number of Units
issued under the Offering, solely to cover over-allotments, if any, and for market stabilization purposes. The Over-Allotment Option may be exercised by the Agent in respect of: (i) Over-Allotment Units at the Offering Price; (ii)
Over-Allotment Warrants at a price of US $[●] per Over-Allotment Warrant; or (iii) any combination of Over-Allotment Units and/or Over-Allotment Warrants, so long as the aggregate number of Over-Allotment Units and Over-Allotment Warrants
does not exceed 15% of the number of Units issued under the Offering (excluding the Over-Allotment Option). Unless the context otherwise requires, references to the Units herein shall include the Over-Allotment Units and references to
Warrants herein shall include the Over-Allotment Warrants. The Common Shares that are included in the Over-Allotment Units are referred to herein as the “Over-Allotment Shares” and the Common Shares issuable upon exercise of the
Over-Allotment Warrants (including Warrants issuable as part of the Over-Allotment Units) are referred to herein as the “Over-Allotment Warrant Shares”. If the Agent exercises the Over-Allotment Option in full under the Maximum Offering for
Over-Allotment Units, the total price to the public will be US $[●], the aggregate Agent’s Commission will be US $[●], and the net proceeds to the Company, before deducting the estimated expenses of the Offering, will be US $[●]. This short
form prospectus qualifies the grant of the Over-Allotment Option and the distribution of the Over-Allotment Units and/or Over-Allotment Warrants. A purchaser who acquires securities forming part of the Agent’s over-allocation position
acquires those securities under this short form prospectus, regardless of whether such over-allocation position is ultimately filled through the exercise of the Over-Allotment Option or through secondary market purchases. See “Plan of Distribution”.
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Agent’s Position
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Minimum Offering
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Maximum Offering
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Exercise Period
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Exercise Price
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Over-
Allotment
Option
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Up to [●]
Over-Allotment Units and/or Over-Allotment Warrants
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Up [●]
Over-Allotment Units
and/or Over-Allotment
Warrants
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From the date of the Agency Agreement to 30 days following the first Closing Date
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US $[●] per
Over-Allotment Unit
and/or US $[●] per
Over-Allotment Warrant
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Broker
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[●]
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[●]
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24 months
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US $[●] per
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Warrants(1) | Broker Warrants | Broker Warrants | following the first | Broker Warrant Share | |||||
Closing Date |
(1)
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Assuming no exercise of the Over-Allotment Option.
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Name of the Person or Company
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Name and Address of Agent
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Charles Federico
David McNally
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Titan Medical Inc.
170 University Avenue, Suite 1000
Toronto, Ontario, Canada
M5H 3B3
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John Schellhorn
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TABLE OF CONTENTS
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IMPORTANT NOTICE ABOUT THE INFORMATION IN THIS SHORT FORM PROSPECTUS
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1
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SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
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2
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CURRENCY PRESENTATION AND EXCHANGE RATE INFORMATION
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5
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DOCUMENTS INCORPORATED BY REFERENCE
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5
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MARKETING MATERIALS
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7
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DOCUMENTS FILED AS PART OF THE REGISTRATION STATEMENT
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7
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THE BUSINESS
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7
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RECENT DEVELOPMENTS
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16
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PRICE RANGE AND TRADING VOLUME OF LISTED SECURITIES
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18
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PRIOR SALES
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21
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DESCRIPTION OF OFFERED SECURITIES
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22
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CAPITALIZATION
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25
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USE OF PROCEEDS
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26
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PLAN OF DISTRIBUTION
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28
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ENFORCEABILITY OF CIVIL LIABILITIES
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30
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RISK FACTORS
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31
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ELIGIBILITY FOR INVESTMENT
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35
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CERTAIN CANADIAN FEDERAL INCOME TAX CONSIDERATIONS
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36
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CERTAIN UNITED STATES FEDERAL INCOME TAX CONSIDERATIONS
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39
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TRANSFER AGENT AND REGISTRAR
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49
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EXPERTS
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49
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LEGAL MATTERS
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49
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●
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the Company’s technology and research and development objectives, including development milestones, estimated costs, schedules for completion and probability of
success;
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●
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the Company’s intention with respect to updating any forward-looking statement after the date on which such statement is made or to reflect the occurrence of
unanticipated events;
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the Company’s expectation with respect to continuing animal study feasibility and commencing human cadaver studies;
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●
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the Company’s expectation that it can in a timely manner produce the appropriate preclinical, and if necessary, clinical data required;
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the Company’s expectation with respect to launching a commercial product in certain jurisdictions;
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the Company’s intentions to develop a robust training curriculum and post-training assessment tools;
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the Company’s plans to develop and commercialize its robotic surgical system and the estimated incremental costs (including the status, cost and timing of
achieving the development milestones disclosed herein);
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the Company’s plans to design, create and refine software for production system functionality of its robotic surgical system and the estimated incremental costs
(including the status, cost and timing of achieving the development milestones disclosed herein);
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the Company’s intentions to complete summative human factors studies and complete the design and development of the system and initiate clinical studies;
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the Company’s intentions with respect to initiating marketing activities following receipt of the applicable regulatory approvals;
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the surgical indications for, and the benefits of, the robotic surgical system;
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the Company’s intention to continue to assess specialized skill and knowledge requirements and recruitment and retention of qualified personnel and partners;
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the Company’s intention to pursue the recruitment of surgeons and hospitals for the required studies and to obtain approval from the IRB (as defined herein) of
each hospital;
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the Company’s belief that the materials and parts necessary for the manufacture of a clinical-grade robotic surgical system will be available in the
marketplace;
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the Company’s filing and prosecution of patent applications to expand its intellectual property portfolio as technologies are developed or refined;
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the Company’s seeking of licensing opportunities to expand its intellectual property portfolio;
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the Company’s expectation that it will be able to finance its continuing operations by accessing public markets for its securities;
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the Company’s intended use of proceeds of any offering of its securities;
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●
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the Company’s intention with respect to not paying any cash dividends on Common Shares in the foreseeable future;
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●
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the Company’s intention to retain future earnings, if any, to finance expansion and growth;
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●
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the projected competitive conditions with respect to the Company’s products;
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●
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the estimated size of the market for robotic surgical systems;
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the potential market for the securities issuable under the Offering; and
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over-allotment options or other transactions which would stabilize or maintain the market price of the Company’s securities.
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●
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Additional Financing and Going Concern
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●
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History of Losses
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●
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Dependence on Key Personnel
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●
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Ability to Attract Qualified Employees to Maintain and Grow Business
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Breach and Loss of Trade Secrets and Other Proprietary Information
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●
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Dependence on Third Parties
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●
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Competition
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Infringement of Intellectual Property Rights
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Intellectual Property – Patents
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Intellectual Property – Trade-marks
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Ability to License Other Intellectual Property Rights
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●
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Current Global Financial Conditions
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●
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Conflicts of Interest
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●
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Results of Operations
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●
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Rapidly Changing Markets Make it Difficult to Forecast Future Operating Results
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●
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Uncertain Market/Uncertain Acceptance of the Company’s Technology/Target Market
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Technological Advancements
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Insurance and Uninsured Risks
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Government Regulation
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Profitability
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●
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Changes in Government Policy
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●
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Changes in Accounting and Tax Rules
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●
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Contingent Liabilities
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●
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Obligations as a Public Company
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●
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The Company Is a “Foreign Private Issuer” Under the U.S. Securities Laws
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●
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The Company May Lose its Status as a Foreign Private Issuer Under the U.S. Securities Laws
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●
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The Company Is an Emerging Growth Company Under the U.S. Securities Laws
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● |
The Company is Probably a PFIC (As Defined Herein) |
●
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Uncertainty as to Product Development and Commercialization Milestones
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Product and Services Not Completely Developed
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●
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Manufacturing Risks
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●
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Reliance on External Suppliers and Development Firms
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●
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Product Defect Risks
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●
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Supplier Risks
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●
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Stock Price Volatility
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●
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Future Share Sales
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●
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Limited Operating History
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●
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Strategic Alliances
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●
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Fluctuating Financial Results
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●
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Effect of Estimates Regarding Milestones
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●
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Currency Fluctuations
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●
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Liquidity of the Common Shares
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●
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Ability of the Company to Maintain Its Stock Exchange Listings
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general business and current global economic conditions;
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future success of current research and development activities;
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achieving development and commercial milestones;
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inability to achieve produce cost targets;
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competition;
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●
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changes to tax rates and benefits;
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●
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the availability of financing;
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the Company’s and competitors’ costs of production and operations;
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●
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the Company’s ability to attract and retain skilled employees;
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●
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the Company’s ongoing relations with its third-party service providers;
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●
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the design of the robotic surgical system and related platforms and equipment;
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the progress and timing of the development of the Company’s robotic surgical system;
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costs related to the development, completion and potential commercialization of the Company’s robotic surgical system;
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●
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receipt of all applicable regulatory approvals/clearances;
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●
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estimates and projections regarding the robotic surgery equipment industry;
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●
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protection of the Company’s intellectual property rights;
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●
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market acceptance of the Company’s systems under development;
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●
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the Company’s ability to meet the continued listing standards of Nasdaq and the TSX; and
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●
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the type of specialized skill and knowledge required to develop the Company’s robotic surgical system and the Company’s access to such specialized skill and
knowledge.
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High (CDN)
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Low (CDN)
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Average (CDN)
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||||||||||
Fiscal years ended
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December 31, 2018
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$
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1.3642
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$
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1.2288
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$
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1.2957
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||||||
December 31, 2017
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$
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1.3743
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$
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1.2128
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$
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1.2986
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1.
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the annual information form of the Company dated March 29, 2019 for the financial year ended December 31, 2018 (the “AIF”);
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2.
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the audited financial statements of the Company as at, and for the financial years ended December 31, 2018 and 2017, together with the notes
thereto and the independent auditor’s reports thereon (the “Annual Financial Statements”);
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3.
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the management’s discussion and analysis of financial condition and results of operations for the financial year ended December 31, 2018
(the “Annual MD&A”);
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4.
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the unaudited condensed interim financial statements of the Company as at, and for the three and six months ended, June 30, 2019, consisting
of the unaudited condensed interim balance sheet of the Company as at June 30, 2019 and the unaudited condensed interim statement of shareholders’ equity and deficit, net and comprehensive loss and cash flows for the three and six months
ended June 30, 2019 and 2018, together with the notes thereto (the “Interim Financial Statements”);
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5.
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the management’s discussion and analysis of financial condition and results of operations for the three and six months ended June 30, 2019
(the “Interim MD&A”);
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6.
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the management information circular dated April 29, 2019 relating to Titan’s annual and special meeting of shareholders on May 29, 2019;
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7.
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the material change report of the Company dated March 6, 2019 in respect of the filing of a preliminary short form prospectus and the
announcement of pricing details for a previous public offering (the “March Offering”);
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8.
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the material change report of the Company dated March 28, 2019 in respect of the filing of a final short form prospectus (the "March
Prospectus") and the closing of the March Offering; and
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9.
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the material change report of the Company dated August 29, 2019 in respect of the Aspire Agreement (as defined herein).
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Milestone Number
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Development Milestones
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Estimated Cost
(in US million $) |
Schedule for
Milestone
Completion
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Comments
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Milestone 1
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a) |
Prototype, test and procure surgeon feedback on revised workstation controls
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b) |
Complete software and hardware change requirements and finalize computer and software architecture for production systems
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Q2 2018 | Completed |
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c) |
Complete revisions to instrument and lens wash system and demonstrate performance
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Milestone 2
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a) |
Complete Camera Insertion Tube (CIT) engineering confidence build based on improved design
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b) |
Complete design of surgeon workstation and patient cart for engineering confidence build
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Q3 2018 | Completed | |
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c) |
Complete and demonstrate full suite of simulation software for beta test
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Milestone Number
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Development Milestones
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Estimated Cost (in US million $) |
Schedule for Milestone
Completion
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Comments
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Milestone 3
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a) |
Complete capital equipment engineering confidence build based on improved design
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Q4 2018
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Completed
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Milestone 4(1)
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a) |
Document results of confidence build unit testing, implement subsystem design improvements and schedule preliminary audit of quality system by European Notified Body
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Q1 2019
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Completed
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Milestone 5(2)
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a) |
Update system design and related hardware and software documentation
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Q2 2019
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Completed
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b) |
Initiate Design Freeze
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Completed
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c) |
Initiate preclinical live animal (swine) and cadaver studies according to final protocols for FDA submittal
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Completed
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d) |
Submit draft protocols to FDA in Q-submission(s) for comment
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Completed
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Milestone 6(3)
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a) |
Complete and document preclinical live animal (swine) and cadaver studies according to final protocols for FDA submittal
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Q3 2019
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Completed
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b) |
Verify production system operation with clinical experts under rigorous formal (summative) human factors evaluation under simulated robotic manipulation exercises
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Completed
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c) |
Complete audits for ISO 13485 Certification
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Completed
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Milestone 7(4)
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a) |
Prepare application for Investigational Device Exemption (IDE)
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5.2(5)
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a) September
2019
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To date, approximately US $2.6 million spent. Estimated cost to complete is approximately US $2.6 million.
|
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b) |
Initiate preparations for IDE studies, including communications with IRB Committees of IDE hospitals
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b) September
2019
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Milestone 8(4)
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Submit IDE application to FDA
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4.1(6)
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a) October 2019
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Moved from Q3 2019
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Milestone Number
|
Development Milestones
|
Estimated Cost (in US million $) |
Schedule for Milestone Completion
|
Comments
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Milestone 9
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a) |
Continue preparations for IDE studies
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11.4(7)
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a) November
2019
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New
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b) |
Obtain ISO 13485 Certification(8)
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b) December
2019
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Moved from Q3
2019
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c) |
Receive IDE approval from FDA(9)
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c) December
2019
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Moved from Q3
2019
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Milestone 10
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a) |
Receive approvals from IRB Committees of IDE hospitals
|
11.0(10)
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Q1 2020
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Moved from Q4
2019
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b) |
Commence human confirmatory studies under IDE protocols for FDA submittal
|
Moved from Q4
2019
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Milestone 11
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a) |
Complete human confirmatory studies and patient follow-up and compile reports from human confirmatory studies
|
7.5(11)
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Q2 2020
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Moved from Q4
2019
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b) |
Submit 510(k) application to FDA
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Moved from Q4
2019
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||
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c) |
Submit Technical File to European Notified Body for review for CE Mark
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Moved from Q4
2019
|
||
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d) |
Ongoing software development and implementation
|
Moved from Q1
2020
|
||
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e) |
Planning and preparation for manufacturing and commercialization
|
Moved from Q1
2020
|
||
Milestone 12
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a) |
Planning and preparation for commercialization
|
TBD
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Q3 2020
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Moved from Q2
2020
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(1)
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The March Prospectus disclosed the estimated cost for Milestone 4 as US $16 million, the actual cost for Milestone 4 was US $16.1 million, being a 0.63% increase from what was disclosed in the March Prospectus. Actual costs
exceeded estimated costs due to minor variances. Milestone 4 was completed in the manner disclosed in the March Prospectus.
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(2)
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The March Prospectus disclosed the estimated cost for Milestone 5 as US $16.9 million, the actual cost for Milestone 5 was US $21.0 million, being a 24.3%
increase from what was disclosed in the March Prospectus. Actual costs exceeded estimated costs due to unanticipated robotic system software issues and design problems related to consumable instruments that interface with the robotic
system and led to delays in the preparation of documentation for the IDE application. These issues also caused delay in the completion of the summative human factor evaluation which was completed in the third quarter of 2019 rather than
as scheduled in the later part of the second quarter of 2019. Other than the submission of the IDE application to FDA, which is discussed further below, Milestone 5 was completed in the manner disclosed in the March Prospectus.
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(3)
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The March Prospectus disclosed the estimated cost for Milestone 6 as US $16.1 million, the actual cost for Milestone 6 was US $13.1 million, being a 18.6% decrease from what was disclosed in the March Prospectus. Actual costs were
less than estimated costs as not all steps were completed in the planned timeframe, with certain steps being delayed to Milestone 9 and beyond, including receipt of the ISO 13485 Certification and the IDE approval. The cause for this
delay is the unanticipated robotic system software issues and design problems related to consumable instruments that interface with the robotic system.
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(4)
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Milestones 7 and 8 together constitute the Company’s next significant milestone.
|
(5)
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Includes research and development costs estimated at approximately US $4.6 million, and general and administrative costs estimated at approximately US $0.6
million. Estimated costs are inclusive of all general and administrative expenses that the Company is aware of in order to complete this Milestone. Other than payment of invoices for work previously performed by its subcontractors, the
Company does not anticipate any other cash outflow requirements in order to complete this Milestone.
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(6) |
Includes research and development costs estimated at approximately US $3.5 million, and general and administrative costs estimated at approximately US $0.6 million. Estimated costs are inclusive of all general and administrative
expenses that the Company is aware of in order to complete this Milestone. The Company does not anticipate any other cash outflow requirements in order to complete this Milestone.
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(7) |
Includes research and development costs estimated at approximately US $10.2 million, and general and administrative costs estimated at approximately US $1.2 million.
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(8) |
The March Prospectus disclosed that obtaining ISO 13485 Certification was expected to occur in the third quarter of 2019.
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(9) |
The March Prospectus disclosed that receipt of IDE approval from the FDA was expected to occur in the third quarter of 2019.
|
(10) |
Includes research and development costs estimated at approximately US $8.7 million, and general and administrative costs estimated at approximately US $2.3 million.
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(11) |
Includes research and development costs estimated at approximately US $4.5 million, and general and administrative costs estimated at approximately US $3.0 million.
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(1)
|
a device that has grandfather marketing status because it was legally marketed prior to May 28, 1976, the date upon which the Medical Device Amendments of 1976 were enacted, or
|
(2)
|
a Class I or II device that has been cleared through the 510(k) process.
|
● |
Florida Hospital Nicholson Center in Celebration, Florida;
|
● |
Columbia University Medical Center in New York, New York; and
|
● |
Institut Hospitalo-Universitaire de Strasbourg (“IHU Strasbourg”) in Strasbourg, France.
|
•
|
GYN and GYN-ONC (8 procedures at Columbia University and Florida Hospital):
|
o
|
Radical Hysterectomy with Bilateral Salpingo Oophorectomy and Bilateral Pelvic / Para-Aortic Node Dissection
|
o
|
Simple Hysterectomy with Bilateral Salpingo Oophorectomy and Bilateral Pelvic Node Dissection
|
o
|
Simple Hysterectomy with Bilateral Salpingo Oophorectomy
|
•
|
Urology (19 procedures at IHU Strasbourg and Florida Hospital):
|
o
|
Hemi-Nephrectomy and Partial Nephrectomy
|
o
|
Prostatectomy (Human Cadaver)
|
o
|
Pyeloplasty
|
o
|
Ureteral-Bladder Anastomosis
|
•
|
General Surgery (14 procedures at IHU Strasbourg and Florida Hospital):
|
o
|
Cholecystectomy (1 Human Cadaver, 5 Live Porcine)
|
o
|
Nissen Fundoplication (1 Human Cadaver, 3 Live Porcine)
|
o
|
Esophagectomy (Human Cadaver)
|
o
|
Gastrectomy
|
o
|
Splenectomy
|
•
|
Colorectal (4 procedures at Florida Hospital):
|
o
|
Colectomy
|
o
|
Low Anterior Resection
|
TSX
|
Nasdaq
|
|||||
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
High (US $)
|
Low (US $)
|
Volume
|
2018
|
||||||
September
|
3.05
|
2.40
|
570,750
|
2.37
|
1.85
|
3,484,916
|
October
|
2.95
|
2.47
|
279,330
|
2.27
|
1.90
|
1,397,121
|
November
|
3.00
|
2.30
|
182,390
|
2.03
|
1.80
|
1,018,750
|
December
|
2.59
|
1.44
|
128,319
|
1.98
|
1.05
|
1,768,093
|
2019
|
||||||
January
|
6.20
|
1.62
|
4,738,600
|
4.65
|
1.19
|
15,319,904
|
TSX
|
Nasdaq
|
|||||
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
High (US $)
|
Low (US $)
|
Volume
|
February
|
6.17
|
4.37
|
3,060,410
|
4.65
|
3.34
|
8,828,793
|
March
|
5.77
|
3.70
|
3,653, 910
|
4.5
|
2.76
|
7,788,646
|
April
|
4.21
|
2.83
|
2,047,860
|
3.14
|
2.12
|
5,874154
|
May
|
3.99
|
3.16
|
1,171,230
|
2.99
|
2.4
|
3,371,969
|
June
|
3.54
|
2.80
|
750, 030
|
2.64
|
2.11
|
2,549,772
|
July
|
3.18
|
2.51
|
421, 000
|
2.50
|
1.9
|
1,905,157
|
August
|
3.50
|
2.40
|
1,073,320
|
2.71
|
1.65
|
4,711,651
|
September 1 - 20
|
3.0
|
2.47
|
750,930
|
2.29
|
2.02
|
3,146,672
|
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
2018
|
|||
September
|
0.01
|
0.01
|
2,000
|
October
|
0.02
|
0.01
|
43,000
|
November
|
0.02
|
0.015
|
37,000
|
December
|
0.01
|
0.01
|
1,000
|
2019
|
|||
January
|
0.015
|
0.015
|
71,500
|
February
|
0.02
|
0.015
|
51,602
|
March
|
-
|
-
|
-
|
April
|
0.01
|
0.005
|
53,250
|
May
|
-
|
-
|
-
|
June
|
-
|
-
|
-
|
July
|
-
|
-
|
-
|
August
|
0.01
|
0.01
|
1,000
|
September 1 - 20
|
0.005
|
0.005
|
14,000
|
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
2018
|
|||
September
|
-
|
-
|
-
|
October
|
0.02
|
0.005
|
232,500
|
November
|
0.025
|
0.005
|
374,000
|
December
|
-
|
-
|
-
|
2019
|
|||
January
|
-
|
-
|
-
|
February
|
0.07
|
0.045
|
187,150
|
March
|
0.065
|
0.02
|
140,600
|
April
|
0.055
|
0.03
|
28,000
|
May
|
0.065
|
0.05
|
116,000
|
June
|
-
|
-
|
-
|
July
|
0.03
|
0.03
|
17,000
|
August
|
0.045
|
0.045
|
10,000
|
September 1 - 20
|
0.55
|
0.03
|
30,000
|
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
2018
|
|||
September
|
0.025
|
0.02
|
65,000
|
October
|
0.015
|
0.005
|
438,700
|
November
|
0.025
|
0.01
|
186,000
|
December
|
-
|
-
|
-
|
2019
|
|||
January
|
0.045
|
0.015
|
176,000
|
February
|
0.04
|
0.02
|
389,000
|
March
|
-
|
-
|
-
|
April
|
0.03
|
0.0197
|
320,000
|
May
|
0.04
|
0.04
|
50,000
|
June
|
-
|
-
|
-
|
July
|
-
|
-
|
-
|
August
|
0.015
|
0.0095
|
100,000
|
September 1 - 20
|
-
|
-
|
-
|
Month
|
High (CDN $)
|
Low (CDN $)
|
Volume
|
2018
|
|||
September
|
0.03
|
0.02
|
170,450
|
October
|
0.08
|
0.04
|
113,460
|
November
|
0.075
|
0.025
|
19,000
|
December
|
0.02
|
0.02
|
1,000
|
2019
|
|||
January
|
0.17
|
0.05
|
381,890
|
February
|
0.155
|
0.075
|
748,420
|
March
|
0.12
|
0.11
|
26,000
|
April
|
0.105
|
0.06
|
348,950
|
May
|
0.105
|
0.07
|
211,300
|
June
|
0.115
|
0.08
|
276,200
|
July
|
0.10
|
0.03
|
2.500
|
August
|
0.115
|
0.085
|
151,500
|
September 1 - 20
|
0.10
|
0.09
|
50,000
|
Date
|
Price Per Common Share
|
Number of Common Shares Issued
|
January 23, 2019
|
US $3.20
|
68,316(1)
|
January 24, 2019
|
US $3.20
|
248,574(1)
|
January 25, 2019
|
US $3.20
|
30,000(1)
|
January 28, 2019
|
US $3.20
|
71,700(1)
|
January 29, 2019
|
US $3.20
|
20,500(1)
|
February 1, 2019
|
US $3.20
|
25,000(1)
|
February 4, 2019
|
US $3.20
|
151,516(1)
|
February 8, 2019
|
US $3.20
|
4,000(1)
|
February 19, 2019
|
US $3.20
|
139,800(1)
|
February 20, 2019
|
US $3.20
|
35,000(1)
|
March 4, 2019
|
US $3.20
|
75,000(1)
|
March 5, 2019
|
US $3.20
|
49,100(1)
|
March 7, 2019
|
US $3.20
|
100,000(1)
|
March 21, 2019
|
US $1.32
|
8,455,882(2)
|
August 30, 2019
|
US $1.99
|
639,837(3)
|
August 30, 2019
|
US $1.69
|
1,777,325(3)
|
(1)
|
Issued pursuant to the exercise of warrants originally issued August 10, 2018
|
(2)
|
Issued pursuant to a short form prospectus of the Company dated March 18, 2019
|
(3)
|
Issued pursuant to a Common Share Purchase Agreement dated August 29, 2019
|
Date
|
Exercise Price per
Common Shares |
Number of Common
Shares Exercisable |
March 21, 2019
|
US $4.00
|
8,455,882(1)
|
(1)
|
Issued pursuant to a short form prospectus of the Company dated March 18, 2018.
|
Date
|
Exercise Price
|
Number of Stock Options Granted
|
December 18, 2018
|
US $1.55
|
50,349
|
February 14, 2019
|
US $3.72
|
40,000
|
May 29, 2019
|
US $3.40
|
253,000
|
June 28, 2019
|
CDN $4.54
|
10,000
|
July 18, 2019
|
CDN $4.54
|
25,719
|
July 19, 2019
|
US $2.20
|
469,420
|
July 19, 2019
|
US $3.40
|
41,273
|
September 9, 2019
|
US $3.72
|
40,000
|
(i)
|
the issuance of Common Shares or securities exchangeable for or convertible into Common Shares to holders of all or substantially all of the Company’s
Common Shares by way of stock dividend or other distribution (other than a “dividend paid in the ordinary course”, as defined in the Warrant Indenture, or a distribution of Common Shares upon the exercise of the Warrants or pursuant
to the exercise of director, officer or employee stock options granted under the Company’s stock option plan);
|
(ii)
|
the subdivision, redivision or change of the Common Shares into a greater number of shares;
|
(iii)
|
the reduction, combination or consolidation of the Common Shares into a lesser number of shares;
|
(iv)
|
the fixing of a record date for the issue of rights, options or warrants to all or substantially all of the holders of the Common Shares under which such
holders are entitled, during a period expiring not more than 45 days after the record date for such issuance, to subscribe for or purchase Common Shares, or securities exchangeable for or convertible into Common Shares, at a price per
share to the holder (or having an exchange or conversion price per share) of less than 95% of the “current market price”, as defined in the Warrant Indenture, for the Common Shares on such record date; and
|
(v)
|
the issuance or distribution to all or substantially all of the holders of the securities of the Company including shares, rights, options or warrants to
acquire shares of any class or securities exchangeable or convertible into any such shares or cash, property or assets and including evidences of indebtedness, or any cash, property or other assets.
|
Description of Capital
|
Outstanding as at
June 30, 2019 (US $) |
Outstanding as at June 30, 2019 after giving effect to the Minimum Offering
(US $)(1)
|
Outstanding as at June 30, 2019 after giving effect to the Maximum Offering
(US $)(1)
|
|||
Share Capital
|
$189,723,070
(31,150,237 Common Shares) |
$[●]
([●] Common Shares) |
$[●]
([●] Common Shares) |
|||
Warrants
|
$27,307,700
(21,203,411 Warrants(3)) |
$[●]
([●] Warrants(3)) |
$[●]
([●] Warrants(3)) |
|||
Contributed Surplus
|
$
|
7,643,817
|
$[●]
|
$[●]
|
||
Common Shares Underlying Stock Options
|
1,187,037 Common Shares
|
1,187,037 Common Shares
|
1,187,037 Common Shares
|
(1)
|
Does not include the issuance or exercise of any options, warrants and broker warrants since June 30, 2019. For details of the share issuances in connection
with such exercises, please see “Prior Sales” in this short form prospectus.
|
(2)
|
Assuming no exercise of the Over-Allotment Option and no exercise of the Broker Warrants to be issued in connection with the Offering. Upon the exercise of
all of the Broker Warrants issuable under the Minimum Offering into Broker Warrant Shares, there would be issued and outstanding [●] Common Shares. Upon the exercise of all of the Broker Warrants issuable under the Maximum Offering
into Broker Warrant Shares, there would be issued and outstanding [●] Common Shares.
|
(3)
|
Assuming no exercise of the Over-Allotment Option and excludes broker warrants issued by the Company. As at September 20, 2019, the Company had issued and
outstanding 1,328,089 broker warrants and it will have [●] broker warrants issued and outstanding in the event of the Minimum Offering and [●] broker warrants issued and outstanding in the event of the Maximum Offering. This assumes
no current holder of a broker warrant exercises any or all of such securities.
|
Approximate Proceeds from the
Minimum Offering
|
Approximate Proceeds from the
Maximum Offering
|
||
Milestone 7(1)
|
US $5.2 million
|
US $5.2 million
|
|
Milestone 8
|
US $4.1 million
|
US $4.1 million
|
|
Milestone 9
|
-
|
US $3.8 million
|
|
Working Capital
|
US $6.9 million
|
US $6.9 million
|
|
Total Net Proceeds(2)
|
US $16.2 million
|
US $ 20.0 million
|
|
(1)
|
The Company estimates that the total cost for Milestone 7 is US $5.2 million. As of the date of this short form prospectus, approximately US $2.6 million has been incurred with respect to Milestone
7while approximately US $2.6 million remains to be incurred. The incurred costs are included in the Company’s accounts payable.
|
(2)
|
Assuming no exercise of the Over-Allotment Option.
|
• |
the Offered Shares and Warrant Shares will, on the date of issue, be qualified investments for trusts governed by registered retirement savings plans (each a “RRSP”), registered education savings plans (each a “RESP”), registered
retirement income funds (each a “RRIF”), registered disability savings plans (each a “RDSP”), deferred profit sharing plans and tax‑free savings accounts (each a “TFSA”), all within the meaning of the Tax Act (collectively, “Plans”)
provided that the Offered Shares and Warrant Shares are listed on a “designated stock exchange” as defined in the Tax Act (which includes the TSX and Nasdaq); and
|
• |
the Warrants will, on the date of issue, be qualified investments for Plans provided that either (i) the Warrants are listed on a “designated stock exchange” as defined in the Tax Act (which includes the TSX and Nasdaq), or
(ii) the Warrant Shares are listed on a “designated stock exchange” as defined in the Tax Act (which includes the TSX and Nasdaq) and the Company is not, and deals at arm’s length with each person who is, an annuitant, a
beneficiary, an employer or a subscriber under or a holder of such Plan.
|
●
|
a citizen or individual resident of the United States;
|
●
|
a corporation (or other entity treated as a corporation for U.S. federal income tax purposes) organized under the laws of the United States, any state thereof or the District of Columbia;
|
●
|
an estate whose income is subject to U.S. federal income taxation regardless of its source; or
|
●
|
a trust that (1) is subject to the primary supervision of a court within the United States and the control of one or more U.S. persons for all substantial decisions or (2) has a valid election in effect under applicable Treasury
Regulations to be treated as a U.S. person.
|
Exhibit
Number |
|
Description
|
3.1
|
*
|
Agency Agreement.
|
3.2
|
*
|
Warrant Indenture
|
|
|
|
|
||
|
|
|
|
||
|
|
|
|
||
|
|
|
|
||
|
|
|
|
||
|
|
|
|
||
|
|
|
|
||
4.8 | ||
4.9 |
||
|
||
5.2
|
*
|
Consent of Borden Ladner Gervais LLP
|
5.3
|
*
|
Consent of Baker & McKenzie LLP
|
|
|
|
|
TITAN MEDICAL INC. | |||
By:
|
/s/ Stephen Randall | ||
Name: Stephen Randall | |||
Title: Chief Financial Officer | |||
Signature
|
|
Capacity
|
|
Date
|
|
|
|
|
|
/s/ David McNally
|
|
President, Chief Executive Officer (Principal
|
|
September 23, 2019
|
David McNally | Executive Officer) and Director |
|||
|
|
|
|
|
|
|
|
|
|
/s/ Stephen Randall
|
|
Chief Financial Officer (Principal Financial
|
|
September 23, 2019
|
Stephen Randall | and Accounting Officer) and Director |
|||
|
|
|
|
|
|
|
|
|
|
/s/ John E. Barker |
|
Director |
|
September 23, 2019
|
John E. Barker |
|
|
|
|
|
|
|
|
|
/s/ John E. Schellhorn |
|
Director |
|
September 23, 2019
|
John E. Schellhorn |
|
|
|
|
|
|
|
|
|
/s/ Charles W. Federico |
|
Director and Chairman |
|
September 23, 2019
|
Charles W. Federico |
|
|
|
|
|
|
|
|
|
/s/ Domenic Serafino |
|
Director |
|
September 23, 2019
|
Domenic Serafino |
|
|
|
|
|
|
|
|
|