FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stent, Carotid

PMA: P050019 · Supplement: S040 · Decision Mar 8, 2024
Classifications
1
FEI Numbers
24
Registration Numbers
24

Basic Information

Device Name
Stent, Carotid
Trade Name
Carotid Wallstent™ Monorail™ Endoprosthesis
PMA Number
P050019
Supplement Number
S040
Device Class
FDA Class 3
Product Code
NIM
Generic Name
Stent, carotid
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
March 8, 2024
Date Received
July 31, 2023
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 the addition of an alternate sterilization site, Synergy Health Ede. B.V. (STERIS) in the Netherlands

Classifications

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

Product Code Device Name
NIM Stent, Carotid