Press Release
TransEnterix Submits 510(k) Application to FDA for SurgiBot System
-- First Patient-Side Robotically Enhanced Laparoscopic Surgery Platform --
"TransEnterix is pleased to deliver on our commitment to file for 510(k)
clearance for the SurgiBot System by mid-2015," said
The SurgiBot System is the first patient-side, robotically enhanced laparoscopy platform. Our goal is to usher in the next wave of minimally invasive surgery by delivering excellent instrument dexterity and precision, surgeon comfort, and minimize patient incisions. The system is also designed to be mobile, minimize reliance on additional staff, and be cost-effective for many types of surgical facilities.
The surgical approach and motions used with the SurgiBot are intended to mimic established laparoscopic surgical techniques. The system utilizes flexible instruments through articulating channels controlled directly by the surgeon, with robotic assistance, from within the sterile field. The flexible nature of the system allows multiple instruments to be introduced and deployed through a single incision.
About
Forward Looking Statements
This press release includes statements relating to 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, including whether we will be able to successfully
commercialize the SurgiBot System and whether the SurgiBot System will
be able to be utilized in a wide variety of surgical facilities with the
potential to deliver critical benefits to surgeons, hospitals and
patients. Factors that could cause our results to differ materially from
those described include, but are not limited to, whether the SurgiBot
System's 510(k) application will be cleared by the U.S.
View source version on businesswire.com: http://www.businesswire.com/news/home/20150601005836/en/
Media Contact:
mnathan@transenterix.com
or
Investor
Contact:
transenterix@westwicke.com
Source:
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