FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pulse Generator

PMA: P180036 · Supplement: S028 · Decision Jun 13, 2024
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
Implantable Pulse Generator
Trade Name
OPTIMIZER® Smart Mini
PMA Number
P180036
Supplement Number
S028
Device Class
FDA Class 3
Product Code
QFV
Generic Name
Implantable pulse generator
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 13, 2024
Date Received
March 20, 2024
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

modifications to the current 1.1.4.3 OPTIMIZER® Smart Mini implantable pulse generator (IPG) Application Software used by the INTELIO Programmer

Classifications

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

Product Code Device Name
QFV Implantable Pulse Generator