INTERSTIM THERAPY SYSTEM
FDA premarket approval P970004/S079 · decided 2010-04-13
Approval details
- PMA number
- P970004
- Supplement
- S079
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- INTERSTIM THERAPY SYSTEM
- Generic name
- Stimulator, electrical, implantable, for incontinence
- Applicant
- Medtronic Neuromodulation
- Date received
- 2010-01-26
- Decision date
- 2010-04-13
- Days to decision
- 77 days
- Decision code
- APPR
- Product code
- EZW
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- APPROVAL FOR A CHANGE TO THE HUB MATERIAL OF THE FORAMEN NEEDLE IN THE MEDTRONIC INTERSTIM ACCESSORY KITS (MODELS 041828, 041829, AND 3065U).
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |