Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Ortho Kinematics, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K173247 Surgical Planning Software version 1.1LLZ2017-11-08 View
510(k) K172327 VMA™ System version 3.0LLZ2017-08-25 View
510(k) K171617 OKI Surgical Planning SoftwareLLZ2017-08-22 View
510(k) K130743 THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLLLZ2013-08-06 View
510(k) K112109 THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLECTION DEVICELLZ2011-12-22 View
↑