Neo Medical SA

Neo Medical SA — FDA 510(k) Submissions

Neo Medical SA has submitted 6 FDA 510(k) premarket notifications since 2017, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Thoracolumbosacral Pedicle Screw System, Intervertebral Fusion Device With Bone Graft, Lumbar, Bone Cement, Posterior Screw Augmentation . Use the specialty filter in the sidebar to narrow results.