Zimmer, Inc.
ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM, MODEL 2357 & 2359
SKU K050121UPC HRS
In Stock
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IIFDA 510(k) Cleared (K050121)
1
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Zimmer, Inc.
Free shipping on orders over $99 · 30-day returns
ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM, MODEL 2357 & 2359 is an FDA 510(k)-cleared medical device (K050121) 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 30, 2005. Regulation: 8.
