DEPUY DURALOC ACETABULAR CUP SYSTEM-ENDURON LINER

DEPUY DURALOC ACETABULAR CUP SYSTEM-ENDURON LINER is an FDA 510(k)-cleared medical device (K983491) manufactured by DePuy Orthopaedics, 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 December 1, 1998. Regulation: 8.