SHAW KNEE MODULAR TIBIAL TRAY-POROUS

SHAW KNEE MODULAR TIBIAL TRAY-POROUS is an FDA 510(k)-cleared medical device (K894937) 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 January 30, 1990. Regulation: 8.