MERCY HIP/KNEE PACK

MERCY HIP/KNEE PACK is an FDA 510(k)-cleared medical device (K896215) manufactured by Westmark, Sterile Packing Systems, Inc. (Sps). This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 12, 1990. Regulation: 8.