Minnetronix Neuro, Inc.

Minnetronix Neuro, Inc. — FDA 510(k) Submissions

Minnetronix Neuro, Inc. has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Retractor, Self-retaining, For Neurosurgery . Use the specialty filter in the sidebar to narrow results.