Spinal Simplicity, LLC

Spinal Simplicity, LLC — FDA 510(k) Submissions

Spinal Simplicity, LLC has submitted 14 FDA 510(k) premarket notifications since 2015, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spinous Process Plate, Sacroiliac Joint Fixation, Posterior Cervical Screw System, Appliance, Fixation, Spinal Intervertebral Body . Use the specialty filter in the sidebar to narrow results.