# K250865: KLS Martin IPS Forearm System

- Pathway: 510(k) (Traditional)
- Applicant: KLS-Martin L.P.
- Decided: Nov 14, 2025 after 238 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: 8 generations back to K962616 (1996). 22 ancestors in all.
No later device cites it as a predicate yet.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222624: KLS Martin LINOS Wrist System, KLS-Martin L.P. (2023) Summary page 5.

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

Source page: https://510kreport.com/device/K250865
Methodology: https://510kreport.com/methodology