MEDTRONIC RESTORE FAMILY IMPLANTABLE NEUROSTIMULATORS
FDA premarket approval P840001/S095 · decided 2007-03-07
Approval details
- PMA number
- P840001
- Supplement
- S095
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- MEDTRONIC RESTORE FAMILY IMPLANTABLE NEUROSTIMULATORS
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2006-12-28
- Decision date
- 2007-03-07
- Days to decision
- 69 days
- Decision code
- APPR
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL FOR A MINOR DESIGN CHANGE TO THE FEEDTHROUGH AND FOR THE USE OF ACETONE FOR THE REMOVAL AND REPLACEMENT OF THE CONNECTOR BLOCK IN THE MANUFACTURING REWORK PROCESS.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |