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GORE® VIATORR® TIPS Endoprosthesis

FDA premarket approval P040027/S090 · decided 2022-02-22

Approval details

PMA number
P040027
Supplement
S090
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GORE® VIATORR® TIPS Endoprosthesis
Generic name
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Applicant
W. L. Gore & Associates, Inc.
Date received
2022-01-20
Decision date
2022-02-22
Days to decision
33 days
Decision code
OK30
Product code
MIR
Advisory committee
Cardiovascular
Expedited review
No
Location
Phonix, AZ
Statement
Removal of cytotoxicity and infrared spectroscopy inspections for incoming components.

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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