PERCUTANEOUS ENDOSCOPIC DISCECTOMY

PERCUTANEOUS ENDOSCOPIC DISCECTOMY is an FDA 510(k)-cleared medical device (K960222) manufactured by Richard Wolf Medical Instruments Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 7, 1996. Regulation: 8.