Evolution Spine

Evolution Spine — FDA 510(k) Submissions

Evolution Spine has submitted 8 FDA 510(k) premarket notifications since 2021, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Integrated Fixation, Lumbar, Appliance, Fixation, Spinal Intervertebral Body, Intervertebral Fusion Device With Integrated Fixation, Cervical, Orthopedic Stereotaxic Instrument . Use the specialty filter in the sidebar to narrow results.