Atlas FDA

GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis

FDA premarket approval P230023 · decided 2024-01-12

Approval details

PMA number
P230023
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
2023-07-19
Decision date
2024-01-12
Days to decision
177 days
Decision code
APPR
Product code
QZK
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
Approval for the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis. This device is indicated for endovascular repair in patients with thoracoabdominal aortic aneurysms and high-surgical risk patients with pararenal aortic aneurysms who have appropriate anatomy.

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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