STRYKER CROSSFLOW ARTHROSCOPY PUMP

STRYKER CROSSFLOW ARTHROSCOPY PUMP is an FDA 510(k)-cleared medical device (K123441) manufactured by Stryker Endoscopy. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 2013. Regulation: 8.