Biomet, Inc.
BIOMET MODULAR FEMORAL REVISION SYSTEM
SKU K090757UPC KWA
In Stock
—
IIIFDA 510(k) Cleared (K090757)
1
Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
BIOMET MODULAR FEMORAL REVISION SYSTEM is an FDA 510(k)-cleared medical device (K090757) manufactured by Biomet, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 24, 2009. Regulation: 8.
