VASCUTEK VASCULAR PROTHESIS VP1200K/50K

VASCUTEK VASCULAR PROTHESIS VP1200K/50K is an FDA 510(k)-cleared medical device (K830016) manufactured by Pacesetter Systems. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 20, 1983. Regulation: 8.