Howmedica Osteonics Corp.
MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM
SKU K024060UPC HWC
In Stock
—
IIFDA 510(k) Cleared (K024060)
1
Free shipping on orders over $99 · 30-day returns
Howmedica Osteonics Corp.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO ASNIS III CANNULATED SCREW SYSTEM is an FDA 510(k)-cleared medical device (K024060) manufactured by Howmedica Osteonics Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2002. Regulation: 8.
