Stryker CrossFlow Integrated Arthroscopy Pump

Stryker CrossFlow Integrated Arthroscopy Pump is an FDA 510(k)-cleared medical device (K191259) manufactured by Stryker Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 2019. Regulation: 8.