FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

System, Endovascular Graft, Aortic Aneurysm Treatment

PMA: P100021 · Supplement: S071 · Decision May 3, 2018
Classifications
1
FEI Numbers
34
Registration Numbers
34

Basic Information

Device Name
System, Endovascular Graft, Aortic Aneurysm Treatment
Trade Name
Talent Occluder
PMA Number
P100021
Supplement Number
S071
Device Class
FDA Class 3
Product Code
MIH
Generic Name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
May 3, 2018
Date Received
April 5, 2018
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Modifications to the stent ring finishing process for the Talent Occluder and Valiant Captivia devices.

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