Biomet, Inc.
AGC REVISION KNEE PROTHESIS
SKU K912245UPC JWH
In Stock
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IIFDA 510(k) Cleared (K912245)
1
Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
AGC REVISION KNEE PROTHESIS is an FDA 510(k)-cleared medical device (K912245) 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 August 18, 1991. Regulation: 8.
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