Intellis Spinal Cord Stimulation Systems
FDA premarket approval P840001/S478 · decided 2020-12-17
Approval details
- PMA number
- P840001
- Supplement
- S478
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Intellis Spinal Cord Stimulation Systems
- Generic name
- Stimulator, spinal-cord, totally implanted for pain relief
- Applicant
- Medtronic Neuromodulation
- Date received
- 2020-11-19
- Decision date
- 2020-12-17
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- LGW
- Advisory committee
- Neurology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Update the surface finishing process of the Header Connector part for the Master Intellis Spinal Cord Stimulation Systems; Model Numbers 97715 and 97716, from a tumble finishing operation to a laser finishing operation. Consolidate two inspection test methods to one test method for the Header Connector.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |