IMPLANT, H.P. CONDYLAR

IMPLANT, H.P. CONDYLAR is an FDA 510(k)-cleared medical device (K781870) manufactured by Dow Corning Corp. Healthcare Industries Materials. 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 8, 1979. Regulation: 8.