HOWMEDICA KINEMATIC TOTAL CONDYLAR KNEE

HOWMEDICA KINEMATIC TOTAL CONDYLAR KNEE is an FDA 510(k)-cleared medical device (K820030) 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 February 4, 1982. Regulation: 8.