Atlas FDA

GORE VIABAHN VBX Balloon Expandable Endoprosthesis

FDA premarket approval P160021/S016 · decided 2019-04-09

Approval details

PMA number
P160021
Supplement
S016
Supplement type
Real-Time Process
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
2018-11-21
Decision date
2019-04-09
Days to decision
139 days
Decision code
APPR
Product code
PRL
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
Approval for new device inspection equipment and modified stent profile acceptance criteria.

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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