FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Endovascular Graft, Aortic Aneurysm Treatment

PMA: P040043 · Supplement: S096 · Decision Oct 31, 2017
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
System, Endovascular Graft, Aortic Aneurysm Treatment
Trade Name
Gore Tag Thoracic Endoprosthesis
PMA Number
P040043
Supplement Number
S096
Device Class
FDA Class 3
Product Code
MIH
Generic Name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
October 31, 2017
Date Received
October 2, 2017
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for updates to the Gore CTAG Thoracic Endoprosthesis Instructions for Use (IFU), including additional language in the Warnings and Precautions and Patient Counseling sections.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MIH System, Endovascular Graft, Aortic Aneurysm Treatment