# K222624: KLS Martin LINOS Wrist System

- Pathway: 510(k) (Traditional)
- Applicant: KLS-Martin L.P.
- Decided: May 25, 2023 after 267 days
- Product code: HRS (Plate, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K962616 (1996). 21 ancestors in all.
5 later devices descend from it; 4 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142906: APTUS Wrist 2.5 System, Medartis AG (2015) Summary page 5.

## Most influential descendants
- K241018: KLS Martin Orthopedic Implants - MR Conditional (2024), 1 descendant of its own
- K254162: KLS Martin Ixos System (2026), 0 descendants of its own
- K250988: KLS Martin Pure Pectus System (2025), 0 descendants of its own
- K250865: KLS Martin IPS Forearm System (2025), 0 descendants of its own
- K250620: KLS Martin Ixos System (2025), 0 descendants of its own

## Indications for use
The KLS Martin LINOS Wrist System is indicated for use in forearm fractures, osteotomies, and arthrodeses. It is intended for adults, and children (2-12 years) and adolescents (12-21 years) in which growth plates have fused or in which growth plates will not be crossed by fixation.

Source page: https://510kreport.com/device/K222624
Methodology: https://510kreport.com/methodology