TRI-LOCK II TITANIUM ACETABULUM PROSTHESIS

TRI-LOCK II TITANIUM ACETABULUM PROSTHESIS is an FDA 510(k)-cleared medical device (K862702) 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 July 29, 1986. Regulation: 8.