InterStim Therapy System, Verify Evaluation System
FDA premarket approval P970004/S409 · decided 2025-01-06
Approval details
- PMA number
- P970004
- Supplement
- S409
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- InterStim Therapy System, Verify Evaluation System
- Generic name
- Stimulator, electrical, implantable, for incontinence
- Applicant
- Medtronic Neuromodulation
- Date received
- 2024-10-23
- Decision date
- 2025-01-06
- Days to decision
- 75 days
- Decision code
- APPR
- Product code
- EZW
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- a change of elemental impurities testing specification, test lab location, and testing frequency on a silicone raw material
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |