Depuy Spine, A Johnson & Johnson Company

Depuy Spine, A Johnson & Johnson Company — FDA 510(k) Submissions

Depuy Spine, A Johnson & Johnson Company has submitted 4 FDA 510(k) premarket notifications since 2007, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Thoracolumbosacral Pedicle Screw System, Cement, Bone, Vertebroplasty, Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis . Use the specialty filter in the sidebar to narrow results.