FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pulse Generator

PMA: P180036 · Supplement: S019 · Decision Jul 21, 2023
Classifications
1
FEI Numbers
2
Registration Numbers
2

Basic Information

Device Name
Implantable Pulse Generator
Trade Name
OPTIMIZER Smart and Smart Mini
PMA Number
P180036
Supplement Number
S019
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
July 21, 2023
Date Received
April 26, 2023
Supplement Type
Real-Time Process
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for updates to the INTELIO Programmer software.

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