Press Release
Asensus Surgical Receives FDA 510(k) Clearance for Articulating Instruments
Instrument platform expected to expand dexterity and add capability to Senhance® Surgical System
“Bringing the benefits of 5 mm articulating instruments to the Senhance Surgical System in the
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Forward-Looking Statements
This press release includes statements relating to the Senhance Surgical System and the FDA 510(k) clearance for articulating instruments. 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 and include whether the benefits of 5 mm articulating instruments to the Senhance Surgical System will widen clinical utility and value of our platform, and whether articulating instruments will expand dexterity and add capabilities to the Senhance Surgical System . For a discussion of the risks and uncertainties associated with the Company’s business, please review our filings with the
View source version on businesswire.com: https://www.businesswire.com/news/home/20210728005560/en/
INVESTOR CONTACT:
invest@asensus.com
or
MEDIA CONTACT:
CG Life
kschaeffer@cglife.com
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