Oxford Performance Materials, Inc.

Oxford Performance Materials, Inc. — FDA 510(k) Submissions

Oxford Performance Materials, Inc. has submitted 3 FDA 510(k) premarket notifications since 2016, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction, Plate, Cranioplasty, Preformed, Non-alterable, Fastener, Fixation, Nondegradable, Soft Tissue . Use the specialty filter in the sidebar to narrow results.