LORD SCREW RING ACETABULAR COMPONENT

LORD SCREW RING ACETABULAR COMPONENT is an FDA 510(k)-cleared medical device (K844028) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 11, 1985. Regulation: 8.