Atlas FDA

GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis

FDA premarket approval P230023/S009 · decided 2025-09-09

Approval details

PMA number
P230023
Supplement
S009
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis
Generic name
Endovascular system for treatment of thoracoabdominal and pararenal aortic lesions
Applicant
W. L. Gore & Associates, Inc.
Date received
2025-08-11
Decision date
2025-09-09
Days to decision
29 days
Decision code
OK30
Product code
QZK
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
implementation of an additional primary supplier of radiopaque markers used in the GORE® EXCLUDER® Iliac Branch Endoprosthesis, Conformable GORE® TAG® Thoracic Endoprosthesis, GORE® TAG® Conformable Thoracic Stent Graft with ACTIVE CONTROL System, GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis, and GORE® TAG® Thoracic Branch Endoprosthesis

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510(k) clearances by this applicant

RecordFirmDate
GORE® Tri-Lobe Balloon Catheter (K250410)W. L. Gore & Associates, Inc.2025-06-02
GORE® PROPATEN® Vascular Graft (K240083)W. L. Gore & Associates, Inc.2024-03-01
GORE® PROPATEN® Vascular Graft (K232312)W. L. Gore & Associates, Inc.2024-01-09
GORE® ACUSEAL Vascular Graft (K233551)W. L. Gore & Associates, Inc.2023-12-19
GORE® ACUSEAL Vascular Graft (K231505)W. L. Gore & Associates, Inc.2023-06-23
GORE BIO-A Tissue Reinforcement (K191773)W. L. Gore & Associates, Inc.2019-07-31
GORE SEAMGUARD Bioabsorbable Staple Line Reinforcement (K181940)W. L. Gore & Associates, Inc.2018-08-17
GORE ENFORM Biomaterial (K173333)W. L. Gore & Associates, Inc.2018-04-05