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

System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment

PMA: P130029 · Supplement: S012 · Decision Feb 17, 2023
Classifications
1
FEI Numbers
14
Registration Numbers
14

Basic Information

Device Name
System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment
Trade Name
Fluency™ Endovascular Stent Graft
PMA Number
P130029
Supplement Number
S012
Device Class
FDA Class 3
Product Code
PFV
Generic Name
System, endovascular graft, arteriovenous (AV) dialysis access circuit stenosis treatment
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
February 17, 2023
Date Received
January 20, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Implementation of an additional stent cutting laser.

Classifications

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

Product Code Device Name
PFV System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment