Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit

Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery Kit is an FDA 510(k)-cleared medical device (K240257) manufactured by Bd. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2024. Regulation: 8.