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Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire) +2 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K241518

by The Magstim Company Limited

Identifiers

510(k) Number
K241518 FDA 510(k)
FDA Product Code
OBP FDA 510(k)
Models / Variants
Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire) FDA 510(k)
Horizon® 3.0 TMS Therapy System (Horizon 3.0 with StimGuide Pro) FDA 510(k)
Horizon® 3.0 TMS Therapy System (Horizon 3.0) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 882.5805 FDA 510(k)
Regulation Number
882.5805 FDA 510(k)
Advisory Committee
Neurology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire) +2 more models by The Magstim Company Limited — Class II — FDA_510K — listed in FDA 510(k) — 3 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
The Magstim Company Limited

Sources (1)

  • FDA 510(k) K241518 24 fields · synced Jun 18, 2026