BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER

BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER is an FDA 510(k)-cleared medical device (K081130) manufactured by Bridgepoint Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 13, 2009. Regulation: 8.