Cleared Traditional

HORIZON TMS Therapy System (K180907) - FDA 510(k) Clearance

Class II Neurology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K180907 · Magstim Company, Ltd. · Neurology device
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Aug 2018
Decision
119d
Days
Class 2
Risk

K180907 is an FDA 510(k) clearance for the HORIZON TMS Therapy System. Classified as Transcranial Magnetic Stimulator (product code OBP), Class II - Special Controls.

Submitted by Magstim Company, Ltd. (Whitland, GB). The FDA issued a Cleared decision on August 3, 2018 after a review of 119 days - within the typical 510(k) review window.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5805 - the FDA neurology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Magstim Company, Ltd. devices

Submission Details

510(k) Number K180907 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 06, 2018
Decision Date August 03, 2018
Days to Decision 119 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 148d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code OBP Transcranial Magnetic Stimulator
Device Class Class 2 - 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.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Neurology devices follow this clearance model.

Regulatory Peers - OBP Transcranial Magnetic Stimulator

All 47
Devices cleared under the same product code (OBP) and FDA review panel - the closest regulatory comparables to K180907.
Nexstim Navigated Brain Therapy (NBT) System 2
K182700 · Nexstim Plc · Mar 2019
HORIZON TMS Therapy System
K182853 · Magstim Company, Ltd. · Mar 2019
Mag Vita TMS Therapy System w/Theta Burst Stimulation
K173620 · Tonica Elektronik A/S · Aug 2018
Apollo TMS Therapy System
K180313 · Mag & More GmbH · May 2018
Brainsway Deep (DTMS) System
K173540 · Brainsway , Ltd. · May 2018