# K181866: MotoCLIP/HiMAX Step Staple Implant System

- Pathway: 510(k) (Special)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Aug 9, 2018 after 28 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: 6 generations back to K902307 (1990). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 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.
- K181410: MotoCLIP/HiMAX Implant System, Crossroads Extremity Systems, LLC (2018) Summary page 4.
- K124022: Speed Shift, Biomedical Enterprises, Inc. (2013) Summary page 4.

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

Source page: https://510kreport.com/device/K181866
Methodology: https://510kreport.com/methodology