InterStim Therapy System (Bowel)
FDA premarket approval P080025/S136 · decided 2017-05-23
Approval details
- PMA number
- P080025
- Supplement
- S136
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- InterStim Therapy System (Bowel)
- Generic name
- Implanted electrical device intended for treatment of fecal incontinence
- Applicant
- Medtronic Neuromodulation
- Date received
- 2017-04-26
- Decision date
- 2017-05-23
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- QON
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Allow the use of an additional laser welder (BATWELDLASER040 aka Sven) for the medium rate (MR) battery case-to-cover welding process at Medtronic Energy and Component Center.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |