Ortho Kinematics, Inc.
Ortho Kinematics, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2017, with 4 FDA device recalls on record.
Top product codes for Ortho Kinematics, Inc.
FDA recalls by Ortho Kinematics, Inc.
- Z-2889-2018 — Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological
- Z-2891-2018 — Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be used to process digital image files.
- Z-2882-2018 — Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intended to be used to process digital image files.
- Z-2890-2018 — Vertebral Motion Analyzer (VMA), VMA DataLink Software.2.3.231, 2.3.232. Product Usage: VMA software is a quantitative imaging software application intended to be used to process digital image files.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ortho Kinematics, Inc.
- K173247 — Surgical Planning Software version 1.1
- K172327 — VMA System version 3.0
- K171617 — OKI Surgical Planning Software
- K133875 — THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.2, THE MOTION NORMALIZER PATIENT HANDLING AND DATA
- K130743 — THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLL
- K112109 — THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLECTION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.