FDA 510(k) Applications Submitted by OXFORD PERFORMANCE MATERIALS

FDA 510(k) Number Submission Date Device Name Applicant
K121818 06/20/2012 OSTEOFAB PATIENT SPECIFIC CRANIAL DEVICE OXFORD PERFORMANCE MATERIALS
K142005 07/23/2014 SpineFab Vertebral Body Replacement (VBR) System OXFORD PERFORMANCE MATERIALS
K133809 12/16/2013 OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE OXFORD PERFORMANCE MATERIALS


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