AOS CANNULATED BONE SCREW SYSTEM

AOS CANNULATED BONE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K014185) manufactured by Advanced Orthopaedic Solutions, 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 February 12, 2002. Regulation: 8.