# K173710: MotoBAND CP Implant System

- Pathway: 510(k) (Special)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Feb 12, 2018 after 70 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K954385 (1996). 63 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 68 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160300: MotoBand (TM) CP Implant System, Crossroads Extremity Systems, LLC (2016) Summary page 4.
- K152306: MotoBand¿ CP Implant System, Crossroads Extremity Systems, LLC (2015) Summary page 5.

## 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

## Recalls of this device
- Sep 19, 2019 · Class II · Z-0212-2020: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

## 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 MTP plates and 2-hole plate may be used with the MotoCLIP™ Implant System.

Source page: https://510kreport.com/device/K173710
Methodology: https://510kreport.com/methodology