PMA supplement
P100044 S018: PROPEL MINI SINUS IMPLANT
FDA PMA supplement · Panel Track · Intersect Ent.
Key facts
| Original PMA | P100044 |
|---|---|
| Supplement number | S018 |
| Supplement type | Panel Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | PROPEL MINI SINUS IMPLANT |
| Generic name | Drug-eluting sinus stent |
| Applicant | Intersect Ent. |
| Product code | OWO |
| Received date | Sep 25, 2015 |
| Decision date | Mar 23, 2016 |
| Docket number | 16M-1123 |
| Notice date | Apr 12, 2016 |
At a glance
- No Expedited review granted
- Yes Approval order on file
- Yes 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: