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

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

PMA: P130029 · Supplement: S013 · Decision Aug 13, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0

Basic Information

Device Name
System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment
Trade Name
FLUENCY PLUS ENDOVASCULAR STENT GRAFT
PMA Number
P130029
Supplement Number
S013
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
August 13, 2025
Date Received
July 18, 2025
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

qualification of an additional manufacturing facility for the stent covering process for the Fluency Plus Endovascular Stent Graft

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