ASNIS 2 SMALL DIAMETER CANNULATED SCREW SYSTEM

ASNIS 2 SMALL DIAMETER CANNULATED SCREW SYSTEM is an FDA 510(k)-cleared medical device (K911398) manufactured by Howmedica 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 June 26, 1991. Regulation: 8.