HipXpert 3D Display and Anchoring Application

HipXpert 3D Display and Anchoring Application is an FDA 510(k)-cleared medical device (K200384) manufactured by Surgical Planning Associates, 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 January 27, 2021. Regulation: 8.