KINEMAX TOTAL KNEE SYSTEM FEMORAL SPACERS

KINEMAX TOTAL KNEE SYSTEM FEMORAL SPACERS is an FDA 510(k)-cleared medical device (K894658) 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 October 19, 1989. Regulation: 8.