NaviNetics D1 Stereotactic System

NaviNetics D1 Stereotactic System is an FDA 510(k)-cleared medical device (K210700) manufactured by Navinetics, 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 June 16, 2021. Regulation: 8.