FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Electrical, Implanted, For Parkinsonian Tremor

PMA: P140009 · Supplement: S122 · Decision Sep 26, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0

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Basic Information

Device Name
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
Trade Name
Infinity™ DBS System
PMA Number
P140009
Supplement Number
S122
Device Class
FDA Class 3
Product Code
MHY
Generic Name
Stimulator, electrical, implanted, for parkinsonian tremor
Medical Specialty
Unknown
Advisory Committee
Neurology
Decision
Approved
Decision Code
APPR
Decision Date
September 26, 2025
Date Received
June 30, 2025
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

approval for an alternate second tier supplier of carbon fiber for use in cathode of the battery

Classifications

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

Product Code Device Name
MHY Stimulator, Electrical, Implanted, For Parkinsonian Tremor