Atlas FDA

Reduced Profile GORE VIABAHN VBX Balloon Expandable Endoprosthesis (RP VBX Device)

FDA premarket approval P160021/S047 · decided 2025-05-20

Approval details

PMA number
P160021
Supplement
S047
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Reduced Profile GORE VIABAHN VBX Balloon Expandable Endoprosthesis (RP VBX Device)
Generic name
Iliac covered stent, arterial
Applicant
W. L. Gore & Associates, Inc.
Date received
2024-11-22
Decision date
2025-05-20
Days to decision
179 days
Decision code
APPR
Product code
PRL
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
use of the Reduced Profile GORE VIABAHN VBX Balloon Expandable Endoprosthesis as a branch component option for the GORE EXCLUDER Thoracoabdominal Branch Endoprosthesis (TAMBE)

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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