PROSTEHSIS, TOTAL KNEE REPLACEMENT

PROSTEHSIS, TOTAL KNEE REPLACEMENT is an FDA 510(k)-cleared medical device (K760334) manufactured by Depuy, 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 August 10, 1976. Regulation: 8.