GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM

GENESIS POROUS TIBIAL TRAYS & REVISION KNEE SYSTEM is an FDA 510(k)-cleared medical device (K953274) manufactured by Smith & Nephew Richards, 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 February 4, 1996. Regulation: 8.