# K130666: Khan Kinetic Treatment (KKT-M2)

- Pathway: 510(k) (Traditional)
- Applicant: Optima Health Solutions International Corporation
- Decided: Jan 23, 2014 after 317 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: 2 generations back to K951217 (1995). 2 ancestors in all.
2 later devices descend from it; 2 cite 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)
- K060043: Khan Kinetic Treatment Device (KKT-M1), Optima Health Solutions International, Inc. (2006) Summary page 1.

## Most influential descendants
- K234036: Sonik Monark 100 (2024), 0 descendants of its own
- K192629: Spinalytics (2019), 0 descendants of its own

## Indications for use
The KKT-M2 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 procedure involves the use of diagnostic imaging that qualifies the misalignment between vertebrae. The treatment is then administered using the KKT-M2 device to deliver precise impulses at a required vector configuration.

Source page: https://510kreport.com/device/K130666
Methodology: https://510kreport.com/methodology