SMITH & NEPHEW CONTINUOUS LOOP FIXATION DEVICE

SMITH & NEPHEW CONTINUOUS LOOP FIXATION DEVICE is an FDA 510(k)-cleared medical device (K052652) 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 October 20, 2005. Regulation: 8.