STRYKER QUIKFLAP STERILE PROCEDURE PACK

STRYKER QUIKFLAP STERILE PROCEDURE PACK is an FDA 510(k)-cleared medical device (K120352) manufactured by Stryker. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 10, 2012. Regulation: 8.