Atlas FDA

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis

FDA premarket approval P160021/S048 · decided 2025-11-24

Approval details

PMA number
P160021
Supplement
S048
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis
Generic name
Iliac covered stent, arterial
Applicant
W. L. Gore & Associates, Inc.
Date received
2025-08-22
Decision date
2025-11-24
Days to decision
94 days
Decision code
APPR
Product code
PRL
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
Approval for a reduced profile balloon catheter delivery system and modified packaging for the 10 and 11mm diameter sizes of the GORE VIABAHN VBX Balloon Expandable 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