# K221395: Footmotion Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Jul 1, 2022 after 49 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). 156 ancestors in all.
No later device cites it as a predicate yet.
0 of 157 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.
- K171510: Footmotion Plating System, Newclip Technics (2017) Summary page 5.
- K121651: Ortholoc 3DI Midfoot/Flatfoot System, Wrightmedicaltechnologyinc (2012) Summary page 5.
- K061808: Darco Locking Bone Plate System, Darco International, Inc. (2006) Summary page 5.
- K132898: A.L.P.S. Calcaneal Plating System, Biomet Manufacturing Corp (2013) Summary page 5.
- K190365: Baby Gorilla/Gorilla Plating System, Paragon 28, Inc. (2019) Summary page 5.
- K143061: Activ Ankle Locking Plating System, Newclip Technics (2015) Summary page 5.
- K173641: Activ Ankle, Newclip Technics (2018) Summary page 5.

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

Source page: https://510kreport.com/device/K221395
Methodology: https://510kreport.com/methodology