InterStim® Therapy System, Verify® Evaluation System
FDA premarket approval P080025/S269 · decided 2022-10-27
Approval details
- PMA number
- P080025
- Supplement
- S269
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- InterStim® Therapy System, Verify® Evaluation System
- Generic name
- Implanted electrical device intended for treatment of fecal incontinence
- Applicant
- Medtronic Neuromodulation
- Date received
- 2022-09-27
- Decision date
- 2022-10-27
- Days to decision
- 30 days
- Decision code
- APPR
- Product code
- QON
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Approval for removal of the applicator sponge from the Interstim Evaluation Lead Kit and updated package labeling for the InterStim Evaluation Lead Kit.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |