P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS

P.F.C. MODULAR KNEE SYSTEM, TIBIAL TRAY-POROUS is an FDA 510(k)-cleared medical device (K892394) manufactured by Johnson & Johnson Professionals, 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 July 18, 1989. Regulation: 8.