FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NeuroStar Advanced Therapy System (All previously cleared models)

K Number: K231926 · Decision Mar 22, 2024
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
65
Applicant Total
8
Review Days
266

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Basic Information

Device Name
NeuroStar Advanced Therapy System (All previously cleared models)
K Number
K231926
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5805
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neuronetics, Inc.
Date Received
June 30, 2023
Decision Date
March 22, 2024
Product Code
OBP
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OBP Transcranial Magnetic Stimulator

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OBP), ordered by most recent decision date.

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Other Clearances by Neuronetics, Inc.

K Number Device Name
K222230 NeuroStar, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar Advanced Therapy System for Mental Health
K220127 NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
K212289 NeuroStar Advanced Therapy for adjunctive treatment of OCD, NeuroStar Advanced Therapy System, NeuroStar TMS Therapy System, NeuroStar Advanced Therapy for Mental Health, NeuroStar
K213543 NeuroStar TMS Therapy System, NeuroStar Advanced Therapy System, NeuroStar, NeuroStar Advanced Therapy for Mental Health
K201158 NeuroStar Advanced Therapy
K161519 NeuroStar TMS Therapy System
K160703 NeuroStar TMS Therapy System