Arthrex, Inc.
MODIFICATION TO: ARTHREX INTERFERENCE SCREW
SKU K071176UPC MAI
In Stock
—
IIFDA 510(k) Cleared (K071176)
1
Free shipping on orders over $99 · 30-day returns
Arthrex, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO: ARTHREX INTERFERENCE SCREW is an FDA 510(k)-cleared medical device (K071176) manufactured by Arthrex, 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 2, 2007. Regulation: 8.
