# K060043: Khan Kinetic Treatment Device (KKT-M1)

- Pathway: 510(k) (Traditional)
- Applicant: Optima Health Solutions International, Inc.
- Decided: Mar 23, 2006 after 76 days
- Product code: LXM (Manipulator, Plunger-Like Joint)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K951217 (1995). 1 ancestor in all.
3 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K951217: Atlas Orthogonal Percussion Insttument, Sweat Chiropractic Clinic (1995) Summary page 1.

## Most influential descendants
- K130666: Khan Kinetic Treatment (KKT-M2) (2014), 2 descendants of its own
- K234036: Sonik Monark 100 (2024), 0 descendants of its own
- K192629: Spinalytics (2019), 0 descendants of its own

## Indications for use
The KKT device is to be used in the aid of management of chronic pain due to non-congenital defects. The device can be used as part of a series of steps in the total care of the patient. The device is to be used for the treatment of vertebral motor units which appear to be fixated. The procedure can involve x-ray analysis that quantifies the lateral and rotational misalignments between the vertebrae. The treatment is then administered using the KKT device to deliver precise impulses at a required vector configuration.

Source page: https://510kreport.com/device/K060043
Methodology: https://510kreport.com/methodology