
Zimmer, Inc.
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TRILOGY ACETABULAR SYSTEM CONSTRAINED LINER, MODEL 6154 SERIES is an FDA 510(k)-cleared medical device (K021826) manufactured by Zimmer, 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 19, 2002. Regulation: 8.