# K181410: MotoCLIP/HiMAX Implant System

- Pathway: 510(k) (Special)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Jun 29, 2018 after 30 days
- Product code: JDR (Staple, 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: 5 generations back to K902307 (1990). 6 ancestors in all.
6 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142727: CrossCLIP Implant System, Orthodiscovery Group, LLC (D.B.A. Crossroads Extremity Systems (2014) Summary page 4.

## Most influential descendants
- K193452: MotoBAND CP Implant System (2020), 3 descendants of its own
- K223342: MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System, DynaMET™ Lesser TMT Fusion System (2023), 2 descendants of its own
- K230591: TriLEAP Plating System (2023), 1 descendant of its own
- K253178: TRILEAP Plating System (2026), 0 descendants of its own
- K190722: TriMAX Implant System (2019), 0 descendants of its own

## Indications for use
The MotoCLIP™/HiMAX™ Implant System is indicated for hand and foot bone fragment osteotomy fixation and joint arthrodesis.

Source page: https://510kreport.com/device/K181410
Methodology: https://510kreport.com/methodology