Depuy, Inc.
AMK LANDMARK REVISION KNEE SYSTEM
SKU K925072UPC JWH
In Stock
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IIFDA 510(k) Cleared (K925072)
1
Free shipping on orders over $99 · 30-day returns
Depuy, Inc.
Free shipping on orders over $99 · 30-day returns
AMK LANDMARK REVISION KNEE SYSTEM is an FDA 510(k)-cleared medical device (K925072) manufactured by Depuy, 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 20, 1994. Regulation: 8.
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