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GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis

FDA premarket approval P230023/S003 · decided 2024-08-13

Approval details

PMA number
P230023
Supplement
S003
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location 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
2024-06-13
Decision date
2024-08-13
Days to decision
61 days
Decision code
APPR
Product code
QZK
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
approval for a manufacturing site W. L. Gore & Associates, Inc. located at 32360 N. North Valley Pkwy Phoenix AZ, 85085-4228 for manufacture of the endoprosthesis sub-assembly

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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