PLUS TOTAL KNEE SYST/PERI POST DESIGN TIBIAL COMP

PLUS TOTAL KNEE SYST/PERI POST DESIGN TIBIAL COMP is an FDA 510(k)-cleared medical device (K901936) manufactured by Orthomet, 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 July 2, 1990. Regulation: 8.