Stryker Corp.

Stryker Corp. — FDA 510(k) Submissions

Stryker Corp. has submitted 124 FDA 510(k) premarket notifications since 1976, of which 121 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Intervertebral Fusion Device With Bone Graft, Lumbar, Neurological Stereotaxic Instrument, Arthroscope, Thoracolumbosacral Pedicle Screw System, Electrosurgical, Cutting & Coagulation & Accessories . Use the specialty filter in the sidebar to narrow results.