OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS

OSTEOTECH NAVICULAR AND CANCELLOUS CANNULATED SCREWS is an FDA 510(k)-cleared medical device (K950652) manufactured by Osteotech, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 21, 1995. Regulation: 8.