PROFIX POSTERIOR-STABILIZED KNEE SYSTEM

PROFIX POSTERIOR-STABILIZED KNEE SYSTEM is an FDA 510(k)-cleared medical device (K954909) 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 January 30, 1996. Regulation: 8.