NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS is an FDA 510(k)-cleared medical device (K800494) manufactured by Depuy, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 17, 1980. Regulation: 8.