TRILOGY ACETABULAR SYSTEM LONGEVITY CROSSLINKED POLYETHYLENE

TRILOGY ACETABULAR SYSTEM LONGEVITY CROSSLINKED POLYETHYLENE is an FDA 510(k)-cleared medical device (K990135) 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 July 11, 1999. Regulation: 8.