RESTOREPRIME NEUROSTIMULATOR,PRIMEADVANCED NEUROSTIMULATOR,ITREL 4 NEUROSTIMULATOR,PRIMEADVANCED SURESCAN MRI NEUROSTIMU
FDA premarket approval P840001/S262 · decided 2014-03-19
Approval details
- PMA number
- P840001
- Supplement
- S262
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- RESTOREPRIME NEUROSTIMULATOR,PRIMEADVANCED NEUROSTIMULATOR,ITREL 4 NEUROSTIMULATOR,PRIMEADVANCED SURESCAN MRI NEUROSTIMU
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2014-02-18
- Decision date
- 2014-03-19
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- CHANGES TO THE BATTERY BURN-IN PROCESS AND INSPECTION METHODS.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |