Ortho Kinematics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Ortho Kinematics, Inc.
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.