Biomet, Inc.
AGC V2 REVISION KNEE SYSTEM
SKU K984054UPC JWH
In Stock
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IIFDA 510(k) Cleared (K984054)
1
Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
AGC V2 REVISION KNEE SYSTEM is an FDA 510(k)-cleared medical device (K984054) manufactured by Biomet, 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 29, 1999. Regulation: 8.
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