FEMORAL AND TIBIAL PLUGS OF INTERAX TOTAL KNEE SYSTEM

FEMORAL AND TIBIAL PLUGS OF INTERAX TOTAL KNEE SYSTEM is an FDA 510(k)-cleared medical device (K980713) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 21, 1998. Regulation: 8.