ACUFEX SCREW CANNULA

ACUFEX SCREW CANNULA is an FDA 510(k)-cleared medical device (K972599) manufactured by Smith & Nephew Endoscopy, 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 September 18, 1997. Regulation: 8.