# K961007: Expert Spine Morphotietry Reference

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Corp.
- Decided: Jul 25, 1996 after 135 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
Longest line of descent: 1 generation back to K890121 (1990). 2 ancestors in all.
17 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K950611: Expert Morphomerty Softward, Lunar Corp. (1995) Summary page 1.
- K890121: Modified DPX Bone Densitometer, Lunar (1990) Summary page 1.

## Most influential descendants
- K011917: Advanced Hip Assessment Software (2001), 16 descendants of its own
- K061561: Hip Structural Analysis Software Option for the Hologic QDR X-Ray Bone Densitometers (2006), 13 descendants of its own
- K072664: GE Lunar Femur Strength Software (2008), 7 descendants of its own
- K082402: Osdx Hip BMD System (2008), 6 descendants of its own
- K121716: TBS Insight (2012), 5 descendants of its own

Source page: https://510kreport.com/device/K961007
Methodology: https://510kreport.com/methodology