Biomet, Inc.
Vanguard 360 Revision Knee System
SKU K143192UPC JWH
In Stock
—
IIFDA 510(k) Cleared (K143192)
1
Free shipping on orders over $99 · 30-day returns
Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
Vanguard 360 Revision Knee System is an FDA 510(k)-cleared medical device (K143192) manufactured by Biomet, 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 February 11, 2015. Regulation: 8.
Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020
Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057