# K171510: Footmotion Plating System

- Pathway: 510(k) (Special)
- Applicant: Newclip Technics
- Decided: Sep 8, 2017 after 107 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). 54 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 56 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161448: Footmotion Plating System, Newclip Technics (2016) Summary page 5.
- K120359: Ortholoc 3DI Hallux System, Wrightmedicaltechnologyinc (2012) Summary page 5.

## Most influential descendants
- K221395: Footmotion Plating System (2022), 0 descendants of its own

## Indications for use
The Footmotion Plating System is intended for arthrodeses, fractures and osteotomies fixation and revision surgeries of the foot in adults.

Source page: https://510kreport.com/device/K171510
Methodology: https://510kreport.com/methodology