MEDTRONIC GT2 FUSION GUIDE WIRES

MEDTRONIC GT2 FUSION GUIDE WIRES is an FDA 510(k)-cleared medical device (K992237) 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 September 8, 1999. Regulation: 8.