# K071347: Vax-D Genesis G2 System

- Pathway: 510(k) (Traditional)
- Applicant: Vax-D Medical Technologies, LLC
- Decided: Oct 5, 2007 after 144 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
Longest line of descent: 3 generations back to K894435 (1989). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053503: Vax-D Genesis System (Therapeutic Table), Vax-D Medical Technologies USA, L.C. (2005) Summary page 1.
- K951622: Vax-D Therapeutic Table, Vat-Tech, Inc. (1996) Summary page 1.
- K001712: 3D Activetrac, The Saunders Group (2000) Summary page 1.
- K844385: Escotek Est Trac 401, Nor-Am Patient Care Products, Inc. (1985) Summary page 1.

## Most influential descendants
- K103248: Integrity Spinal Care System (2011), 0 descendants of its own

## Indications for use
This therapy provides a primary treatment modality for the management of pain and disability for patients suffering with spinal pain. It has been found to provide relief in a variety of conditions involving anatomical dysfunctions of the spine that generate localized pain as well as peripheral radiation, including patients with protruding or herniated intervertebral discs as well as those with acute facet problems and sciatica.

Source page: https://510kreport.com/device/K071347
Methodology: https://510kreport.com/methodology