HI-TORQUE EXTRA S'PORT GUIDEWIRE

HI-TORQUE EXTRA S'PORT GUIDEWIRE is an FDA 510(k)-cleared medical device (K021285) manufactured by Guidant 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 May 1, 2002. Regulation: 8.