FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P130029 · Supplement: S004 · Decision Aug 24, 2016
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 PLUS ENDOVASCULAR STENT GRAFT
PMA Number
P130029
Supplement Number
S004
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
Approved
Decision Code
APPR
Decision Date
August 24, 2016
Date Received
February 12, 2016
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for a manufacturing site located at Sterigenics Belgium Petit-Rechain S.A., Zoning Industriel de petit-Rechain, Avenue Andre Ernst 21, Petit-Rechain, Verviers, 4800, Belgium, for contract sterilization.

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