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

Shunt, Portosystemic, Endoprosthesis

PMA: P930031 · Supplement: S072 · Decision Jun 14, 2023
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Shunt, Portosystemic, Endoprosthesis
Trade Name
WALLSTENT™ TIPS Endoprosthesis with Unistep Plus™ Delivery System
PMA Number
P930031
Supplement Number
S072
Device Class
FDA Class 3
Product Code
MIR
Generic Name
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
June 14, 2023
Date Received
June 1, 2023
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Upgrading the control system for the furnace system at the Boston Scientific Corporation (BSC) Galway facility.

Classifications

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

Product Code Device Name
MIR Shunt, Portosystemic, Endoprosthesis