CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT

CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT is an FDA 510(k)-cleared medical device (K000062) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 6, 2000. Regulation: 8.