PMA supplement
P080025 S251: InterStim® Therapy System, Verify® Evaluation System (SNS Bowel)
FDA PMA supplement · Real-Time Process · Medtronic Neuromodulation
Key facts
| Original PMA | P080025 |
|---|---|
| Supplement number | S251 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | InterStim® Therapy System, Verify® Evaluation System (SNS Bowel) |
| Generic name | Implanted electrical device intended for treatment of fecal incontinence |
| Applicant | Medtronic Neuromodulation |
| Product code | QON |
| Received date | Feb 15, 2022 |
| Decision date | May 12, 2022 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: