NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI

NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI is an FDA 510(k)-cleared medical device (K884789) manufactured by Protek, 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 February 7, 1989. Regulation: 8.