NEW JERSEY FEMORAL RESURFACING COMPONENT

NEW JERSEY FEMORAL RESURFACING COMPONENT is an FDA 510(k)-cleared medical device (K842233) manufactured by Endomedics, 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 July 19, 1984. Regulation: 8.