Turnkey Intergration USA, Inc.
MODIFIED FREEMAN REVISION ACETABULAR CUP
SKU K902111UPC KWA
In Stock
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IIIFDA 510(k) Cleared (K902111)
1
Free shipping on orders over $99 · 30-day returns
Turnkey Intergration USA, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFIED FREEMAN REVISION ACETABULAR CUP is an FDA 510(k)-cleared medical device (K902111) manufactured by Turnkey Intergration USA, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on August 21, 1990. Regulation: 8.
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