MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT

MEDTRONIC CLEARVIEW INTRAVASCULAR ARTERIOTOMY SHUNT is an FDA 510(k)-cleared medical device (K993677) manufactured by Medtronic Vascular. 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 16, 2000. Regulation: 8.