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

Shunt, Portosystemic, Endoprosthesis

PMA: P040027 · Supplement: S044 · Decision Jun 11, 2015
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
S044
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 11, 2015
Date Received
May 14, 2015
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

IMPLEMENT A CHANGE IN THE TEST METHOD USED FOR RECEIVING ACCEPTANCE ACTIVITIES FOR RAW MATERIALS.

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