# K190722: TriMAX Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Crossroads Extemity Systems, LLC
- Decided: Aug 16, 2019 after 149 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: 12 generations back to K962616 (1996). 128 ancestors in all.
No later device cites it as a predicate yet.
0 of 129 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181410: MotoCLIP/HiMAX Implant System, Crossroads Extremity Systems, LLC (2018) Summary page 4.
- K152072: CrossRoads Screw System, Crossroads Extremity Systems, LLC (2015) Summary page 4.
- K153622: First Ray Internal Bone Staple System, First Ray, LLC (2016) Summary page 4.
- K163440: Stealth Staple System, First Ray, LLC (2017) Summary page 4.

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

Source page: https://510kreport.com/device/K190722
Methodology: https://510kreport.com/methodology