MOUNTAIN VIEW, Calif., March 8 /PRNewswire/ -- Axis Surgical Technologies, Inc., announced today that it has received 510(k) clearance from the Food and Drug Administration to market their C-MOR(TM) Visualization Device for use in diagnostic and operative arthroscopic and endoscopic procedures. The self-contained portable direct-imaging tool provides illumination and visualization of an interior cavity through either a natural or surgical opening. The ergonomic lightweight device offers practitioners the convenience of endoscopic visualization and efficient one-handed operability that can be employed in hospital outpatient departments, ambulatory surgery centers, and office surgery suites.
“This 510(k) clearance allows for commercialization of the C-MOR(TM) and we are excited to begin execution of our sales strategy. This significant milestone is a welcomed achievement for our team and the orthopedic and sports medicine community”, says Seddiqui.
Axis Surgical Technologies, Inc. of Mountain View, CA, is a medical device company founded on the principle of developing and manufacturing innovative diagnostic and therapeutic products in the areas of orthopedics and spine. The company focuses on creating minimally invasive surgical technologies that combine the world’s most advanced CMOS technology and cutting-edge catheter solutions to create medical imaging systems and therapeutic devices.
CONTACT: Sophia Gran, Marketing Coordinator of Axis Surgical Technologies,
Inc., +1-650-968-3800 X 5600, sgran@axissurgical.com
