# K024171: Vidar Bone Track System Software

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Mar 4, 2003 after 76 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Agfa IMPAX OT3000 Orthopedic Display Station: named in the summary without a submission number

## Indications for use
Bone Track software provides pre-operative digital implant templating to facilitate the selection and ordering of orthopedic implants. The software allows for a semi-automatic ordering process, by printing a pick list, which can be used by the physician to order orthopedic components directly from the manufacturer. The software also tracks those components and provide post-operative patient follow-up all in a digital environment. The software will be provided on a stand-alone or hospital network workstation.

Source page: https://510kreport.com/device/K024171
Methodology: https://510kreport.com/methodology