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Neuronetics receives 510(k) clearance for NeuroSite Coil Placement Accessory
The Fly

Neuronetics receives 510(k) clearance for NeuroSite Coil Placement Accessory

Neuronetics announced the U.S. Food and Drug Administration 510(k) clearance of NeuroSite Coil Placement Accessory, a tool that simplifies measurement and coil positioning during NeuroStar transcranial magnetic stimulation treatments. This proprietary accessory, designed with versatility and provider convenience in mind, seamlessly integrates with both legacy and new NeuroStar systems and further enhances efficiency and patient experience.

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