FDA PMA FDA Class 3 Approved 🇺🇸 United States

System, Endovascular Graft, Aortic Aneurysm Treatment

PMA: P120006 · Supplement: S028 · Decision Oct 13, 2017
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
System, Endovascular Graft, Aortic Aneurysm Treatment
Trade Name
Ovation iX Abdominal Stent Graft System
PMA Number
P120006
Supplement Number
S028
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 13, 2017
Date Received
July 19, 2017
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the use of a thermoformed tray for packaging of the Ovation iX Aortic Body, Iliac Limb, and the associated delivery systems.

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