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GORE VIATORR TIPS Endoprosthesis with Controlled Expansion

FDA premarket approval P040027/S081 · decided 2020-12-04

Approval details

PMA number
P040027
Supplement
S081
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GORE VIATORR TIPS Endoprosthesis with Controlled Expansion
Generic name
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Applicant
W. L. Gore & Associates, Inc.
Date received
2020-11-24
Decision date
2020-12-04
Days to decision
10 days
Decision code
OK30
Product code
MIR
Advisory committee
Cardiovascular
Expedited review
No
Location
Phonix, AZ
Statement
Implementation of process changes in the manufacturing of the Controlled Expansion Sleeve of the GORE VIATORR TIPS Endoprosthesis with Controlled Expansion.

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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