SMITH & NEPHEW ULTRABRAID SUTURE

SMITH & NEPHEW ULTRABRAID SUTURE is an FDA 510(k)-cleared medical device (K041216) manufactured by Smith & Nephew, 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 June 6, 2004. Regulation: 8.