
Zimmer, Inc.
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PERIARTICULAR LOCKING PLATES AND SCREWS, MODEL 2358 SERIES is an FDA 510(k)-cleared medical device (K051098) 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 6, 2005. Regulation: 8.