VERASENSE for Stryker Triathlon

VERASENSE for Stryker Triathlon is an FDA 510(k)-cleared medical device (K200665) manufactured by Orthosensor, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2020. Regulation: 8.