Zimmer Trabecular
EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM
SKU K050766UPC HWE
In Stock
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IFDA 510(k) Cleared (K050766)
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Free shipping on orders over $99 · 30-day returns
Zimmer Trabecular
Free shipping on orders over $99 · 30-day returns
EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEM is an FDA 510(k)-cleared medical device (K050766) manufactured by Zimmer Trabecular. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 25, 2005. Regulation: 8.
