MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT

MEDTRONIC CLEAR INTRAVACULAR ARTERIOTOMY SHUNT is an FDA 510(k)-cleared medical device (K120612) manufactured by Medtronic, Inc.. 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 24, 2012. Regulation: 8.