Neurosplint
Aug 2015
252d
Neurospectrum, LLC
1
Total
1
Cleared
0
Denied
Neurospectrum, LLC — FDA 510(k) Submissions
Neurospectrum, LLC has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Orthosis, Limb Brace . Use the specialty filter in the sidebar to narrow results.
1 devices