P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT

P.F.C. MOD TOTAL KNEE/CONDYL 3 FEM COMP TIB INSERT is an FDA 510(k)-cleared medical device (K924340) manufactured by Johnson & Johnson Orthopaedics, 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 January 24, 1994. Regulation: 8.