Neuralytix iD3 System (NTX-9001)
Jun 2025
213d
Neuralytix, LLC
1
Total
1
Cleared
0
Denied
Neuralytix, LLC — FDA 510(k) Submissions
Neuralytix, LLC has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Neurosurgical Nerve Locator . Use the specialty filter in the sidebar to narrow results.
1 devices