Oxford Performance Materials

Oxford Performance Materials — FDA 510(k) Submissions

Oxford Performance Materials has submitted 3 FDA 510(k) premarket notifications since 2013, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Cranioplasty, Preformed, Non-alterable, Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction, Spinal Vertebral Body Replacement Device . Use the specialty filter in the sidebar to narrow results.