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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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