GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM

GENESIS POSTERIOR STABILIZED (P/S) KNEE SYSTEM is an FDA 510(k)-cleared medical device (K946088) 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 August 7, 1995. Regulation: 8.