Cleared Traditional

Brainsway Deep TMS System

K203735 · Brainsway , Ltd. · Neurology
Apr 2021
Decision
123d
Days
Class 2
Risk

About This 510(k) Submission

K203735 is an FDA 510(k) clearance for the Brainsway Deep TMS System, a Transcranial Magnetic Stimulator (Class II — Special Controls, product code OBP), submitted by Brainsway , Ltd. (Jerusalem, IL). The FDA issued a Cleared decision on April 23, 2021, 123 days after receiving the submission on December 21, 2020. This device falls under the Neurology review panel. Regulated under 21 CFR 882.5805.

Submission Details

510(k) Number K203735 FDA.gov
FDA Decision Cleared SESE
Date Received December 21, 2020
Decision Date April 23, 2021
Days to Decision 123 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF

Device Classification

Product Code OBP — Transcranial Magnetic Stimulator
Device Class Class II — Special Controls
CFR Regulation 21 CFR 882.5805
Definition A Transcranial Magnetic Stimulator Is A Device That Delivers Brief Duration, Rapidly Alternating, Or Pulsed, Magnetic Fields To Induce Electrical Currents That Are Directed At Spatially Discrete Regions Of The Cerebral Cortex For The Treatment Of Major Depressive Disorder.