Atlas FDA

EXCLUDER AAA Endoprosthesis

FDA premarket approval P020004/S159 · decided 2018-10-24

Approval details

PMA number
P020004
Supplement
S159
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
EXCLUDER AAA Endoprosthesis
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
W. L. Gore & Associates, Inc.
Date received
2018-09-26
Decision date
2018-10-24
Days to decision
28 days
Decision code
OK30
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Phonix, AZ
Statement
Implementation of a new film wrapping machine for use in the manufacturing of the GORE EXCLUDER AAA Endoprosthesis and GORE EXCLUDER AAA Endoprosthesis.

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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