Mighty Oak Medical, Inc.

Mighty Oak Medical, Inc. — FDA 510(k) Submissions

Mighty Oak Medical, Inc. has submitted 5 FDA 510(k) premarket notifications since 2015, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Pedicle Screw Placement Guide, Orthosis, Spinal Pedicle Fixation, Posterior Cervical Screw Placement Guide . Use the specialty filter in the sidebar to narrow results.