510(k) K220177
K220177 is an FDA 510(k) premarket notification submitted by Magnus Medical, Inc. for the device "Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K". The FDA issued a decision of Substantially Equivalent on Sep 1, 2022. The device falls under product code OBP (Transcranial Magnetic Stimulator), a Class II device regulated under 21 CFR 882.5805.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 1, 2022
- Date Received
- Jan 21, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transcranial Magnetic Stimulator
- Device Class
- Class II
- Regulation Number
- 882.5805
- Review Panel
- NE
- Submission Type
- 510(k)
A transcranial magnetic stimulator is a device that delivers brief duration, rapidly alternating, or pulsed, magnetic fields to induce electrical currents that are directed at spatially discrete regions of the cerebral cortex for the treatment of major depressive disorder.