GORE® EXCLUDER® Conformable AAA Endoprosthesis
FDA premarket approval P200030/S023 · decided 2025-12-05
Approval details
- PMA number
- P200030
- Supplement
- S023
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- GORE® EXCLUDER® Conformable AAA Endoprosthesis
- Generic name
- SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Applicant
- W. L. Gore and Associates, Inc.
- Date received
- 2025-09-08
- Decision date
- 2025-12-05
- Days to decision
- 88 days
- Decision code
- APPR
- Product code
- MIH
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Phonix, AZ
- Statement
- Approval for modification of the primary sewn tubular sleeve manufacturing process, a change to the primary sleeve attachment fiber, and a change to the proximal primary sleeve attachment pattern for the GORE® EXCLUDER® Conformable AAA Endoprosthesis.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| GORE® ENFORM Biomaterial (K222919) | W. L. Gore and Associates, Inc. | 2022-12-19 |
| GORE Tri-Lumen Catheter (K180919) | W. L. Gore and Associates, Inc. | 2018-10-05 |
| GORE Molding and Occlusion Balloon Catheter (K172567) | W. L. Gore and Associates, Inc. | 2018-01-31 |