# K223342: MotoBAND™ CP Implant System: DynaBunion™ 4D Minimal-incision Bunion System, DynaMET™ Lesser TMT Fusion System

- Pathway: 510(k) (Traditional)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Mar 30, 2023 after 149 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: 11 generations back to K954385 (1996). 72 ancestors in all.
2 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)
- K193452: MotoBAND CP Implant System, Crossroads Extemity Systems, LLC (2020) Summary page 3.
- K173710: MotoBAND CP Implant System, Crossroads Extremity Systems, LLC (2018) Summary page 5.

## Most influential descendants
- 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 includes DynaBunion™ 4D Minimal-incision Bunion System and DynaMet™ Lesser TMT Fusion System, which include plates and screws 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. DynaBunion™ 4D Minimal-incision Bunion System and DynaMet™ Lesser TMT Fusion plates are compatible with fracture fixation staples from the MotoCLIP™/HiMAX™ Implant System cleared in K142727, K181410 and K193452.

Source page: https://510kreport.com/device/K223342
Methodology: https://510kreport.com/methodology