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GORE VIATORR TIPS

FDA premarket approval P040027/S052 · decided 2016-11-29

Approval details

PMA number
P040027
Supplement
S052
Supplement type
Special (Immediate Track)
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
GORE VIATORR TIPS
Generic name
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Applicant
W. L. Gore & Associates, Inc.
Date received
2016-11-07
Decision date
2016-11-29
Days to decision
22 days
Decision code
APPR
Product code
MIR
Advisory committee
Cardiovascular
Expedited review
No
Location
Phonix, AZ
Statement
Approval for an update to the Instructions for Use to indicate that in VIATORR® devices with controlled expansion, ultrasonic visualization of the lumen of the graft-lined region may be difficult through 7 days or greater post-implantation.

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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