DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional

DePuy Synthes Craniomaxillofacial Neuro Devices - MR Conditional is an FDA 510(k)-cleared medical device (K192702) manufactured by Synthes (USA) Products, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2020. Regulation: 8.