510(k) · Neurology

ClearPoint System (Software Version 3.0)

by ClearPoint Neuro, Inc.

ClearPoint System (Software Version 3.0) is an AI-enabled medical device from ClearPoint Neuro, Inc. that the U.S. FDA cleared through 510(k) K243657 on January 24, 2025. Its lead review panel is Neurology and its primary product code is HAW (Neurological Stereotaxic Instrument).

See also FDA-cleared AI neurology devices in 2025, all FDA AI clearances in 2025, top neurology AI devices.

Key facts

Submission numberK243657
Pathway510(k)
Date of final decision
Company (FDA list)ClearPoint Neuro, Inc.
Lead review panelNeurology
Primary product codeHAW — Neurological Stereotaxic Instrument
Applicant (openFDA)ClearPoint Neuro, Inc.
Applicant locationSolana Beach, CA, US
Device classClass 2
Regulation number21 CFR 882.4560
Decision codeSESE
Submission typeTraditional

Source: FDA AI-Enabled Medical Devices list and openFDA.

What this means

A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. ClearPoint System (Software Version 3.0) went through this pathway (K243657).

openFDA lists it as a Class 2 device under 21 CFR 882.4560. Class II devices are moderate risk and are subject to general and special controls.

Product code HAW covers 8 devices on the FDA AI list. By decision date, this device is #7 of 8 under that code. ClearPoint Neuro, Inc. has 3 AI-enabled devices on the list, and the Neurology panel accounts for 73 in total.

Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.

Similar devices (product code HAW)

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