MEDTRONIC RESTORE FAMILY IMPLANTABLE NEUROSTIMULATORS
FDA premarket approval P840001/S100 · decided 2008-02-29
Approval details
- PMA number
- P840001
- Supplement
- S100
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MEDTRONIC RESTORE FAMILY IMPLANTABLE NEUROSTIMULATORS
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2007-10-05
- Decision date
- 2008-02-29
- Days to decision
- 147 days
- Decision code
- APPR
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL FOR A NEW COMPONENT VENDOR FOR TWO INTEGRATED CIRCUITS (ICS) USED ON THE HYBRID IN THE RESTORE FAMILY OF DEVICES.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |