PMA supplement
P010020 S029: AMS ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER (ABS)
FDA PMA supplement · 135 Review Track For 30-Day Notice · Boston Scientific Corp
Key facts
| Original PMA | P010020 |
|---|---|
| Supplement number | S029 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Trade name | AMS ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER (ABS) |
| Generic name | Implanted fecal incontinence device |
| Applicant | Boston Scientific Corp |
| Product code | MIP |
| Received date | Feb 27, 2015 |
| Decision date | Feb 4, 2016 |
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: