# K010249: CD Horizon Spinal System

- Pathway: 510(k) (Special)
- Applicant: Medtronic Sofamor Danek, Inc.
- Decided: Feb 23, 2001 after 28 days
- Product code: MNH (Orthosis, Spondylolisthesis Spinal Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
239 later devices descend from it; 2 cite it directly.
0 of 240 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
- K014296: CD Horizon Spinal System (2002), 237 descendants of its own
- K090714: Vertex Reconstruction System, Vertex Select Reconstruction System (2009), 233 descendants of its own
- K111510: CD Horizon Spinal System (2011), 128 descendants of its own
- K121630: Range Spinal System (2012), 127 descendants of its own
- K110522: Vertex Reconstruction System, Vertex Select Reconstruction System (2011), 106 descendants of its own

Source page: https://510kreport.com/device/K010249
Methodology: https://510kreport.com/methodology