OARtrac System with Patient Specific Reusable Universal PSD Sensors

OARtrac System with Patient Specific Reusable Universal PSD Sensors is an FDA 510(k)-cleared medical device (K162954) manufactured by Radiadyne, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 31, 2017. Regulation: 8.