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GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE

FDA premarket approval P130006/S018 · decided 2015-06-02

Approval details

PMA number
P130006
Supplement
S018
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
Generic name
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment
Applicant
W. L. Gore & Associates, Inc.
Date received
2015-05-04
Decision date
2015-06-02
Days to decision
29 days
Decision code
OK30
Product code
PFV
Advisory committee
Cardiovascular
Expedited review
No
Location
Flagstaff, AZ
Statement
CHANGE IN THE HEAT TREATMENT MANUFACTURING PROCEDURE, THE USE OF A NEW CONTAINER CLOSURE SYSTEM, AS WELL AS THE ADDITION OF TWO SUPPLIERS FOR A PROCESSING AID.

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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