FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P240023 · Supplement: S004 · Decision Dec 11, 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
WRAPSODY® Cell-Impermeable Endoprosthesis
PMA Number
P240023
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
December 11, 2025
Date Received
November 14, 2025
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

approval of the revised protocol for the post-approval study (PAS) referenced above. The PAS protocol has been submitted to comply with the conditions of approval outlined in our approval order for P240023

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