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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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