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

Iliac Covered Stent, Arterial

PMA: P160024 · Supplement: S001 · Decision Jul 19, 2017
Classifications
1
FEI Numbers
12
Registration Numbers
12

Basic Information

Device Name
Iliac Covered Stent, Arterial
Trade Name
LifeStream Balloon Expandable Vascular Covered Stent
PMA Number
P160024
Supplement Number
S001
Device Class
FDA Class 3
Product Code
PRL
Generic Name
Iliac covered stent, arterial
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
July 19, 2017
Date Received
June 19, 2017
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Upgrade the sterilization control system for sterilization line #1 at Bard Regional Sterilization, Covington Facility.

Classifications

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

Product Code Device Name
PRL Iliac Covered Stent, Arterial