KNEE, TOTAL, FEMORAL & TIBIAL

KNEE, TOTAL, FEMORAL & TIBIAL is an FDA 510(k)-cleared medical device (K780904) 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 June 21, 1978. Regulation: 8.