# K001712: 3D Activetrac

- Pathway: 510(k) (Traditional)
- Applicant: The Saunders Group
- Decided: Aug 31, 2000 after 87 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.
17 later devices descend from it; 7 cite it directly.
0 of 18 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
- K031862: Spinerx-LDM (2003), 9 descendants of its own
- K053223: Triton/Tru-Trac/TX/Triton DTS Traction (2006), 8 descendants of its own
- K023160: DRX5000 (2002), 4 descendants of its own
- K151640: Eltrac 471 (2015), 1 descendant of its own
- K071347: Vax-D Genesis G2 System (2007), 1 descendant of its own

Source page: https://510kreport.com/device/K001712
Methodology: https://510kreport.com/methodology