We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Implanet has announced FDA 510(k) clearance of its ...
Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera™ SC – Porous Titanium Cervical Interbody ...