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Wrightmedicaltechnologyinc
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PROCOTYL-E ACETABULAR SYSTEM is an FDA 510(k)-cleared medical device (K043073) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on May 3, 2005. Regulation: 8.