# K923792: Quantec Spinal Measuement System

- Pathway: 510(k) (Traditional)
- Applicant: Quantec Image Processing, Ltd.
- Decided: Apr 20, 1994 after 631 days
- Product code: LDK (Device, Sensing, Optical Contour)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K230463: NSite Scoliosis Assessment App (2023), 0 descendants of its own
- K232023: Momentum Spine (2023), 0 descendants of its own
- K183485: CryoVizion System (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K923792
Methodology: https://510kreport.com/methodology