Press Release
TransEnterix Receives Response from the FDA on SurgiBot 510(k) Submission
"The FDA's decision is extremely disappointing. We are in the process of
reviewing all aspects of the FDA's communication," said
First Quarter Financial and Operating Results Conference Call
To listen to the conference call on your telephone, please dial, 888-427-9419 for domestic callers and 719-457-1035 for international callers and reference TransEnterix Call approximately ten minutes prior to the start time. To access the live audio webcast or archived recording, use the following link http://ir.transenterix.com/events.cfm. The replay will be available on the Company's website.
About
Forward-Looking Statements
This press release includes statements relating to the ALF-X® System,
the SurgiBot™ 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. For a discussion of the risks and
uncertainties associated with
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