Ortho Kinematics, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Ortho Kinematics, Inc. has 6 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 6 cleared submissions from 2011 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ortho Kinematics, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Nov 08, 2017
Surgical Planning Software version 1.1
Radiology
33d
Cleared
Aug 25, 2017
VMA™ System version 3.0
Radiology
24d
Cleared
Aug 22, 2017
OKI Surgical Planning Software
Radiology
82d
Cleared
Jan 17, 2014
THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.2, THE...
Radiology
28d
Cleared
Aug 06, 2013
THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0
Radiology
140d
Cleared
Dec 22, 2011
THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA...
Radiology
153d