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Zimmer, Inc.
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PERIARTICULAR LOCKING PLATES AND SCREWS, SERIES 2358 AND 2359 is an FDA 510(k)-cleared medical device (K043560) 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 January 20, 2005. Regulation: 8.