# K000826: Prodigy Lateral View Software

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Corp.
- Decided: Apr 14, 2000 after 31 days
- Product code: KGI (Densitometer, Bone)
- Device class: 2
- Regulation: 21 CFR 892.1170
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023554: Dual-Energy Vertebral Assessment View Software (2002), 6 descendants of its own
- K103475: Spineanalyer Model Sapoc (2011), 2 descendants of its own
- K052581: Lunar Idxa (2005), 1 descendant of its own
- K252718: Lunar Astra (2026), 0 descendants of its own
- K171435: VirtuOst Vertebral Fracture Assessment (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K000826
Methodology: https://510kreport.com/methodology