# K210060: CoLink Mfx Implant System

- Pathway: 510(k) (Traditional)
- Applicant: In2bones USA, LLC
- Decided: Mar 12, 2021 after 60 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: 16 generations back to K962616 (1996). 149 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 151 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163293: Colink™ Plating System, In2bones USA, LLC (2017) Summary page 5.
- K181113: CoLink™ Afx Plating System, In2bones USA, LLC (2018) Summary page 5.
- K152974: ORTHOLOC® 3Di Foot Plating Reconstruction System, Wrightmedicaltechnologyinc (2015) Summary page 5.

## Most influential descendants
- K261154: CoLink® & CoLag® Non-Sterile Screws (2026), 0 descendants of its own

## Indications for use
The CoLink® Mfx Plating System is intended for stabilization and fixation of fractures, revision procedures, joint fusion, osteotomies and reconstruction in the midfoot bones of the foot, including repair of Lis Franc injuries, in both pediatric and adult patients.

Source page: https://510kreport.com/device/K210060
Methodology: https://510kreport.com/methodology