# K193452: MotoBAND CP Implant System

- Pathway: 510(k) (Special)
- Applicant: Crossroads Extemity Systems, LLC
- Decided: Jan 10, 2020 after 28 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: 10 generations back to K954385 (1996). 71 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 75 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173710: MotoBAND CP Implant System, Crossroads Extremity Systems, LLC (2018) Summary page 4.
- K181410: MotoCLIP/HiMAX Implant System, Crossroads Extremity Systems, LLC (2018) Summary page 4.

## Most influential descendants
- 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

## Indications for use
The MotoBAND™ CP Implant System is indicated for stabilization and fixation of fresh fractures, revision procedures, joint fusion and reconstruction of small bones of the hand, feet, wrist, ankles, fingers and toes. When used for these indications, the MotoBAND™ Implant System with the exception of the 2-hole plate may be used with the MotoCLIP™/HiMAX™ Implant System.

Source page: https://510kreport.com/device/K193452
Methodology: https://510kreport.com/methodology