Flospine

Flospine — FDA 510(k) Submissions

Flospine has submitted 4 FDA 510(k) premarket notifications since 2014, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Appliance, Fixation, Spinal Intervertebral Body, Intervertebral Fusion Device With Bone Graft, Cervical, Spinous Process Plate, Thoracolumbosacral Pedicle Screw System . Use the specialty filter in the sidebar to narrow results.