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GORE VIABAHN VBX BALLOON EXPANDABLE ENDOPROSTHESIS

FDA premarket approval P160021 · decided 2017-01-27

Approval details

PMA number
P160021
Trade name
GORE VIABAHN VBX BALLOON EXPANDABLE ENDOPROSTHESIS
Generic name
Iliac covered stent, arterial
Applicant
W. L. Gore & Associates, Inc.
Date received
2016-07-05
Decision date
2017-01-27
Days to decision
206 days
Decision code
APPR
Product code
PRL
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
Approval for the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of de novo or restenotic lesions found in iliac arteries with reference vessel diameters ranging from 5mm - 13mm and lesion lengths up to 110mm, including lesions at the aortic bifurcation.

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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