# K031871: Autobone

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Europe
- Decided: Jun 20, 2003 after 3 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K871859 (1987). 5 ancestors in all.
58 later devices descend from it; 3 cite it directly.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972399: Advantage Windows Volume Rendering Option, Ge Medical Systems, Inc. (1997) Summary page 2.
- K002519: Vitrea 2, Version 2.1, Vital Images, Inc. (2000)

## Most influential descendants
- K060779: Advance Vessel Analysis II (2006), 55 descendants of its own
- K061370: Cardiq Fusion (2006), 51 descendants of its own
- K103465: Synapse 3D Cardiac Tools (2011), 20 descendants of its own
- K120636: Synapse 3D Cardiac Tools (2012), 19 descendants of its own
- K092747: Philips Comprehensive Cardiac Analysis (Cca) - Plaque Assessment Tool (2009), 19 descendants of its own

## Indications for use
The AutoBone option is a software package that is intended to facilitate segmentation of bony structures from abdominal and extremity CT Angiography data. It runs on Advantage Workstations, revision 4.1 or higher.

Source page: https://510kreport.com/device/K031871
Methodology: https://510kreport.com/methodology