FDA 510(k) Applications Submitted by Leigh Ayres

FDA 510(k) Number Submission Date Device Name Applicant
K080069 01/10/2008 DIMERTEST AMERICAN DIAGNOSTICA, INC.
K161052 04/14/2016 OsteoFab Patient Specific Facial Device OXFORD PERFORMANCE MATERIALS, INC.
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
K052124 08/05/2005 ACTICLOT, MODEL 824 AMERICAN DIAGNOSTICA, INC.
K133809 12/16/2013 OSTEOFAB PATIENT SPECIFIC FACIAL DEVICE OXFORD PERFORMANCE MATERIALS
K033457 10/30/2003 M2 COMPATIBLE MICROKERATOME BLADE MICRO SPECIALTIES, INC.


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