LINK ENDO MODEL REVISION CUP

LINK ENDO MODEL REVISION CUP is an FDA 510(k)-cleared medical device (K943986) manufactured by Turnkey Intergration USA, 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 4, 1995. Regulation: 8.