# K152306: MotoBand¿ CP Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Crossroads Extremity Systems, LLC
- Decided: Dec 11, 2015 after 119 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: 7 generations back to K954385 (1996). 61 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 69 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083447: Memometal Anchorage Bone Plate System, Models PLSS/PLSL, PLP10/PLP20/PLP30/PLP40/PLP50, Memometal Technologies (2009) Summary page 4.
- K131657: Flower Small and Medium Implant Set, Flower Orthopedics Corporation (2013) Summary page 4.
- K123562: Flower Small and Medium Bone Implants, Flower Orthopedics Corporation (2013) Summary page 4.

## Most influential descendants
- K160300: MotoBand (TM) CP Implant System (2016), 6 descendants of its own
- K173710: MotoBAND CP Implant System (2018), 4 descendants of its own
- 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

## 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.

Source page: https://510kreport.com/device/K152306
Methodology: https://510kreport.com/methodology