THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLL— 510(k) K130743

Substantially Equivalent

Ortho Kinematics, Inc.

FDA 510(k) clearance K130743 for THE KINEGRAPH VMA (VERTEBRAL MOTION ANALYZER) SOFTWARE VERSION 2.0; THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLL, Substantially Equivalent on 2013-08-06. Applicant: Ortho Kinematics, Inc..

Clearance details

Applicant: Ortho Kinematics, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2013-03-19
Decision date: 2013-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.