PMA
P210032: GORE TAG Thoracic Branch Endoprosthesis (TBE Device)
FDA PMA · SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT · W. L. Gore & Associates, Inc.
Key facts
| PMA number | P210032 |
|---|---|
| Trade name | GORE TAG Thoracic Branch Endoprosthesis (TBE Device) |
| Generic name | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT |
| Applicant | W. L. Gore & Associates, Inc. |
| Owner/operator | W. L. GORE & ASSOCIATES, INC. |
| Product code | MIH |
| Approval date | May 13, 2022 |
| Docket number | 22M-0813 |
| Notice date | May 17, 2022 |
| Establishment registration | 2017233 |
| FEI number | 2017233 |
At a glance
- 10–99 Supplements
- Jul 13, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 100–999 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: