# K022585: Kimax Qma

- Pathway: 510(k) (Traditional)
- Applicant: Medical Metrics, Inc.
- Decided: Oct 11, 2002 after 67 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 4 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K112109: The Kinegraph Vma Software, the Motion Normalizer Patient Handling and Data Collection Device (2011), 10 descendants of its own
- K130743: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.0; the Motion Normalizer Patient Handling and Data Coll (2013), 9 descendants of its own
- K133875: The Kinegraph Vma (Vertebral Motion Analyzer) Software Version 2.2, the Motion Normalizer Patient Handling and Data (2014), 8 descendants of its own
- K172327: VMA™ System version 3.0 (2017), 7 descendants of its own
- K192109: KOALA (2019), 6 descendants of its own

## Indications for use
KIMAX QMATM is a quantitative imaging software application. It is designed for physicians and clinical professionals who are interested in the analysis of motion in medical images, particularly in musculoskeletal images. KIMAX QMATM permits users to review static and dynamic digital images acquired from a variety of radiographic sources. It also facilitates quantitative assessment of motion in radiographic images. Information about the motion of selected objects, such as bone structures, can be generated and presented in the form of a “motion analysis” report containing graphics, charts and text.

Source page: https://510kreport.com/device/K022585
Methodology: https://510kreport.com/methodology