DEPUY DURALOC ACETABULAR CUP SYSTEM

DEPUY DURALOC ACETABULAR CUP SYSTEM is an FDA 510(k)-cleared medical device (K972596) 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 November 11, 1997. Regulation: 8.