PMA supplement
P210032 S015: GORE TAG Thoracic Branch Endoprosthesis (TBE Device)
FDA PMA supplement · Panel Track · W. L. Gore & Associates, Inc.
Key facts
| Original PMA | P210032 |
|---|---|
| Supplement number | S015 |
| Supplement type | Panel Track |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | GORE TAG Thoracic Branch Endoprosthesis (TBE Device) |
| Generic name | Endovascular System for Treatment of Ascending Aorta and Aortic Arch Lesions |
| Applicant | W. L. Gore & Associates, Inc. |
| Product code | SDZ |
| Received date | Aug 26, 2024 |
| Decision date | Apr 11, 2025 |
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: