NEEDLES AND SUTURES, SILK & NYLON

NEEDLES AND SUTURES, SILK & NYLON is an FDA 510(k)-cleared medical device (K760158) manufactured by Alcon Laboratories. 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 August 18, 1976. Regulation: 8.