Willow 24 Guidewire

Willow 24 Guidewire is an FDA 510(k)-cleared medical device (K260537) manufactured by Arbor Endovascular, LLC. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 18, 2026. Regulation: 8.