Smith & Nephew, Inc.
GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT
SKU K032295UPC JWH
In Stock
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IIFDA 510(k) Cleared (K032295)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT is an FDA 510(k)-cleared medical device (K032295) 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 August 20, 2003. Regulation: 8.
