Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K

Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K is an FDA 510(k)-cleared medical device (K220177) manufactured by Magnus Medical, 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 August 31, 2022. Regulation: 8.