FDA PMA FDA Class 3 Approved 🇺🇸 United States

Stimulator, Electrical, Implanted, For Parkinsonian Tremor

PMA: P140009 · Supplement: S070 · Decision Jul 15, 2021
Classifications
1
FEI Numbers
30
Registration Numbers
30

Basic Information

Device Name
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
Trade Name
St. Jude Medical Clinician Programmer Application, St. Jude Medical Patient Controller Application, St. Jude Medical In
PMA Number
P140009
Supplement Number
S070
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
July 15, 2021
Date Received
June 15, 2021
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for labeling updates to include additional clarification language related to magnets within consumer goods and electronic devices.

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