DEPUY M. KUROSAKA ADVANGE MANGNUM REV. INTERFERENCE SCREWS

DEPUY M. KUROSAKA ADVANGE MANGNUM REV. INTERFERENCE SCREWS is an FDA 510(k)-cleared medical device (K960704) manufactured by Depuy, 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 June 5, 1996. Regulation: 8.