Steerant™ Super Stiff Guidewire

Steerant™ Super Stiff Guidewire is an FDA 510(k)-cleared medical device (K232570) 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 October 23, 2023. Regulation: 8.