FDA PMA FDA Class 3 Approved 🇺🇸 United States

Shunt, Portosystemic, Endoprosthesis

PMA: P040027 · Supplement: S019 · Decision Sep 15, 2010
Classifications
1
FEI Numbers
10
Registration Numbers
10

Basic Information

Device Name
Shunt, Portosystemic, Endoprosthesis
Trade Name
GORE VIATORR TIPS ENDOPROSTHESIS
PMA Number
P040027
Supplement Number
S019
Device Class
FDA Class 3
Product Code
MIR
Generic Name
SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
September 15, 2010
Date Received
February 12, 2010
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR AUTOMATING THE LOADING OF THE ACCESS SLEEVE AND TO USE AN ALTERNATE MATERIAL VENDOR.

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