Press Release
TransEnterix Finalizes FDA Submission Process Related to SurgiBot System 510(k) Application
- Continue to anticipate SurgiBot FDA clearance by the end of the first quarter of 2016 -
- Strengthens balance sheet with
-
Completes FDA Response.
TransEnterix has successfully completed its response to theU.S. Food and Drug Administration (FDA) related to the pending 510(k) application submitted for clearance of the company's SurgiBot™ System. -
Strengthens Balance Sheet. Since
September 30, 2015 , the Company has raised$18 million (1) in net proceeds at an average price of$3.23 per share under its$25 million "at-the-market" (ATM) equity sales facility that was established inFebruary 2015 . There is no further availability under this facility. The proceeds from these sales will be utilized to continue to support investments for the commercialization of the ALF-X® system inEurope , as well as the SurgiBot inthe United States , followingFDA clearance. -
Files New ATM Facility. Following the successful completion of
the prior ATM facility, the Company has entered into a new ATM
facility that allows it the option to raise up to
$43.6 million in equity from time to time throughJanuary 2017 . The Company has no obligation to sell any shares under this facility.
"We are pleased to have completed our response to the
(1)Includes trades that have been processed but not yet settled as of the date of this press release.
About
Forward Looking Statements
This press release includes statements relating to the SurgiBot System,
the ALF-X® System and our current regulatory and commercialization plans
for these products. These statements and other statements regarding our
future plans and goals constitute "forward looking statements" within
the meaning of Section 27A of the Securities Act of 1933 and Section 21E
of the Securities Exchange Act of 1934, and are intended to qualify for
the safe harbor from liability established by the Private Securities
Litigation Reform Act of 1995. Such statements are subject to risks and
uncertainties that are often difficult to predict, are beyond our
control, and which may cause results to differ materially from
expectations, including whether we will achieve clearance for the
SurgiBot System from the
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Media Contact:
mnathan@transenterix.com
or
Investor
Contact:
transenterix@westwicke.com
Source:
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