WHITESIDE ORTHOLOC TOTAL HIP FEMORAL

WHITESIDE ORTHOLOC TOTAL HIP FEMORAL is an FDA 510(k)-cleared medical device (K842559) 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 December 19, 1984. Regulation: 8.