MODIFIED PROFILE II ACETABULAR CUP PROSTHESIS

MODIFIED PROFILE II ACETABULAR CUP PROSTHESIS is an FDA 510(k)-cleared medical device (K901087) 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 May 6, 1990. Regulation: 8.