Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing

Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing is an FDA 510(k)-cleared medical device (K151932) manufactured by Stryker Corporation. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 30, 2016. Regulation: 8.