FDA 510(k) Applications Submitted by ORTHO DEVELOPMENT

FDA 510(k) Number Submission Date Device Name Applicant
K141001 04/18/2014 ALPINE HIP STEM; ALPINE HA HIP STEM ORTHO DEVELOPMENT
K111936 07/08/2011 ORTHO DEVLOPMENT CERAMIC FEMORAL HEAD ORTHO DEVELOPMENT
K111965 07/11/2011 VUSION(R) OS ORTHO DEVELOPMENT
K103384 11/18/2010 ESCALADE ACETABULAR CUP SYSTEM ORTHO DEVELOPMENT
K103837 12/30/2010 BALANCED KNEE SYSTEM REVISION OFFSET TIBIA ORTHO DEVELOPMENT


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