# K951217: Atlas Orthogonal Percussion Insttument

- Pathway: 510(k) (Traditional)
- Applicant: Sweat Chiropractic Clinic
- Decided: Nov 21, 1995 after 249 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
No predicates in its family tree.
4 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K060043: Khan Kinetic Treatment Device (KKT-M1) (2006), 3 descendants of its own
- 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

Source page: https://510kreport.com/device/K951217
Methodology: https://510kreport.com/methodology