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Implanted Subcortical Electrical Stimulator (Motor Disorders)
FDA product code MRU · Class f · Unknown
189
Registered devices
2,909
Adverse events
2
Recalls
0
510(k) clearances
Devices with this code
MEDTRONIC® DBS™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.MEDTRONIC® DBS™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.SenSight™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.ACTIVA® Therapy — MEDTRONIC, INC.N/A — MEDTRONIC, INC.NA — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.Percept™ PC BrainSense™ — MEDTRONIC, INC.Assess Review ™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.NA — MEDTRONIC, INC.NA — MEDTRONIC, INC.MEDTRONIC® DBS™ — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.DBS™ — MEDTRONIC, INC.N/A — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.NA — MEDTRONIC, INC.N'Vision — MEDTRONIC, INC.N/A — MEDTRONIC, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-03-30 | Medtronic Neuromodulation | The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system. |
| 2013-02-08 | Medtronic Neuromodulation | There is a potential for lead damage due to the use of the lead cap provided in DBS and Dystonia kits. Medtronic has received reports of DBS leads being damage |
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