Aesculap Implant System, Inc.
COLUMBUS REVISION KNEE SYSTEM
SKU K083772UPC JWH
In Stock
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IIFDA 510(k) Cleared (K083772)
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Free shipping on orders over $99 · 30-day returns
Aesculap Implant System, Inc.
Free shipping on orders over $99 · 30-day returns
COLUMBUS REVISION KNEE SYSTEM is an FDA 510(k)-cleared medical device (K083772) manufactured by Aesculap Implant System, 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 June 3, 2009. Regulation: 8.
