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FDA 510(k) Applications Submitted by ORTHO KINEMATICS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171617
06/01/2017
OKI Surgical Planning Software
Ortho Kinematics, Inc.
K172327
08/01/2017
VMAÖ System version 3.0
Ortho Kinematics, Inc.
K130743
03/19/2013
THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLL
ORTHO KINEMATICS, INC.
K112109
07/22/2011
THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLECTION DEVICE
ORTHO KINEMATICS, INC.
K133875
12/20/2013
THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.2, THE MOTION NORMALIZER PATIENT HANDLING AND DATA
ORTHO KINEMATICS, INC.
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