AXS Lift Intracranial Base Catheter

AXS Lift Intracranial Base Catheter is an FDA 510(k)-cleared medical device (K253032) manufactured by Stryker Neurovascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 10, 2026. Regulation: 8.