Crux Vena Cava Filter System, femoral; Crux Vena Cava Filter System, jugular

Crux Vena Cava Filter System, femoral; Crux Vena Cava Filter System, jugular is an FDA 510(k)-cleared medical device (K150262) manufactured by Volcano Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 2, 2015. Regulation: 8.