Smith & Nephew, Inc.
SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM
SKU K121627UPC MEH
In Stock
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IIFDA 510(k) Cleared (K121627)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
SMITH & NEPHEW REDAPT REVISION FEMORAL SYSTEM is an FDA 510(k)-cleared medical device (K121627) manufactured by Smith & Nephew, 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 October 14, 2012. Regulation: 8.
