# K002371: K-Centrum Anterior Spinal Fixation System

- Pathway: 510(k) (Abbreviated)
- Applicant: Spineology, Inc.
- Decided: Sep 15, 2000 after 50 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
299 later devices descend from it; 3 cite it directly.
0 of 300 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
- K011556: Macs Hma Anterior Spinal Stabilization System (2001), 293 descendants of its own
- K032059: Modification to Macs Modular Anterior Construct System (2003), 250 descendants of its own
- K070387: Expedium Spine System (2007), 248 descendants of its own
- K102249: Expedium Spine System (2010), 218 descendants of its own
- K111571: Viper Systems (2011), 203 descendants of its own

Source page: https://510kreport.com/device/K002371
Methodology: https://510kreport.com/methodology