FDA PMA FDA Class 3 Approved 🇺🇸 United States

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

PMA: P170042 · Supplement: S011 · Decision Mar 24, 2022
Classifications
1
FEI Numbers
14
Registration Numbers
14

Basic Information

Device Name
System, Endovascular Graft, Arteriovenous (Av) Dialysis Access Circuit Stenosis Treatment
Trade Name
Covera™ Vascular Covered Stent
PMA Number
P170042
Supplement Number
S011
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
March 24, 2022
Date Received
August 20, 2021
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Labeling Change - PAS
Expedited Review
N

Advisory Committee Statement

Approval for an update to the labeling to include the 36-month data on patients enrolled in the AVeNEW IDE extended follow-up study.

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