FDA 510(k) Applications Submitted by Oxford Performance Materials, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K190915 04/09/2019 OsteoFab Suture Anchors Oxford Performance Materials, Inc.
K161052 04/14/2016 OsteoFab Patient Specific Facial Device OXFORD PERFORMANCE MATERIALS, INC.
K180064 01/09/2018 OsteoFab Patient Specific Cranial Device Oxford Performance Materials, Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact