STRYKER STERI-SHIELD FLYTE HYBRID TOGAS

STRYKER STERI-SHIELD FLYTE HYBRID TOGAS is an FDA 510(k)-cleared medical device (K141095) manufactured by Stryker Corporation. 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 25, 2014. Regulation: 8.