HJD CALCAR REPLACEMENT PROSTHESIS

HJD CALCAR REPLACEMENT PROSTHESIS is an FDA 510(k)-cleared medical device (K881769) manufactured by Richards Medical Co., 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 June 21, 1988. Regulation: 8.