Medacta International
GMK REVISION HYBRID LINERS
SKU K111283UPC JWH
In Stock
—
IIFDA 510(k) Cleared (K111283)
1
Free shipping on orders over $99 · 30-day returns
Medacta International
Free shipping on orders over $99 · 30-day returns
GMK REVISION HYBRID LINERS is an FDA 510(k)-cleared medical device (K111283) manufactured by Medacta International. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 26, 2011. Regulation: 8.
