Restore, Itrel, Synergy and Intellis Spinal Cord Stimulation Systems and Pisces, Specify
FDA premarket approval P840001/S443 · decided 2019-09-27
Approval details
- PMA number
- P840001
- Supplement
- S443
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Restore, Itrel, Synergy and Intellis Spinal Cord Stimulation Systems and Pisces, Specify
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2019-08-30
- Decision date
- 2019-09-27
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Update the titanium dioxide paste specification as well as the receiving inspection procedure, allowing a new test method to be implemented and detect both aluminum oxide and titanium dioxide.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |