Master InterStim Therapy System, Verify Evaluation System
FDA premarket approval P970004/S268 · decided 2018-07-03
Approval details
- PMA number
- P970004
- Supplement
- S268
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- Master InterStim Therapy System, Verify Evaluation System
- Generic name
- Stimulator, electrical, implantable, for incontinence
- Applicant
- Medtronic Neuromodulation
- Date received
- 2018-04-04
- Decision date
- 2018-07-03
- Days to decision
- 90 days
- Decision code
- APPR
- Product code
- EZW
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Minneapolis, MN
- Statement
- Approval of new models A510 and A520 programmer applications and TH90 kit for INS; update of programming software for models A511 and A521 programmer applications for ENS; labeling revisions.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| SureTune4 Software (DEN210003) | Medtronic Neuromodulation | 2021-08-23 |