SUTRALENE POLYPROPYLENE SUTURES

SUTRALENE POLYPROPYLENE SUTURES is an FDA 510(k)-cleared medical device (K070243) manufactured by Visionary Medical Supplies, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 16, 2007. Regulation: 8.