STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE

STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE is an FDA 510(k)-cleared medical device (K955599) manufactured by Stryker Corp.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 21, 1996. Regulation: 8.