510(k) Neurology Devices

FDA 510(k) Cleared Neurology Devices

This page lists all 6185 medical devices in the Neurology specialty that have been submitted to the FDA through the 510(k) premarket notification process. EEG systems, neurostimulators, robotic surgical navigation and neuromonitoring.

• 6132 devices cleared as substantially equivalent to a predicate device.
• Average time to FDA decision: 148 days.
• Records available from 1976 to the present.
• Filter by product code using the sidebar to narrow results by device type.