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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact