MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN

MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN is an FDA 510(k)-cleared medical device (K872788) manufactured by Uresil 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 September 24, 1987. Regulation: 8.