STRYKER KNIFELIGHT

STRYKER KNIFELIGHT is an FDA 510(k)-cleared medical device (K100884) manufactured by Howmedica Osteonics Corp.. 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 24, 2010. Regulation: 8.