Stryker Universal Neuro III System: UN III AXS Screw, UN III AXS Screwdriver Blade

Stryker Universal Neuro III System: UN III AXS Screw, UN III AXS Screwdriver Blade is an FDA 510(k)-cleared medical device (K151387) manufactured by Stryker. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 23, 2015. Regulation: 8.