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GORE VIABAHN ENDOPROSTHESIS

FDA premarket approval P040037/S074 · decided 2015-01-08

Approval details

PMA number
P040037
Supplement
S074
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
GORE VIABAHN ENDOPROSTHESIS
Generic name
STENT, SUPERFICIAL FEMORAL ARTERY
Applicant
W. L. Gore & Associates, Inc.
Date received
2014-10-14
Decision date
2015-01-08
Days to decision
86 days
Decision code
APPR
Product code
NIP
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
APPROVAL FOR THE ADDITION OF A 7.5 CM ENDOPROSTHESIS LENGTH IN 5-8 MM AND 9 MM DIAMETER CONFIGURATIONS, WITH AND WITHOUT HEPARIN, ON BOTH THE 0.035 GUIDEWIRE CATHETER (75CM AND 120CM LENGTH) AND THE 0.014/0.018 GUIDEWIRE CATHETER (120CM LENGTH).

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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