MedCAD® AccuStride™ System

MedCAD® AccuStride™ System is an FDA 510(k)-cleared medical device (K252064) manufactured by Medcad. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 26, 2026. Regulation: 8.