# K010292: DRX 2000

- Pathway: 510(k) (Traditional)
- Applicant: Axiom Worldwide, Inc.
- Decided: May 1, 2001 after 90 days
- Product code: ITH (Equipment, Traction, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K022602: DRX3000 (2003), 4 descendants of its own
- K060735: DRX9000 True Spinal Decompression System (2006), 3 descendants of its own
- K243775: True Non-Surgical Spinal Decompression System (DRX9000-SL) (2025), 0 descendants of its own
- K130249: Integrity Spinal Care System 3.0 (2014), 0 descendants of its own
- K073132: Model D Disc Force (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K010292
Methodology: https://510kreport.com/methodology