# K161448: Footmotion Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Oct 31, 2016 after 159 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: 10 generations back to K954385 (1996). 52 ancestors in all.
5 later devices descend from it; 4 cite it directly.
0 of 58 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 5.
- K121651: Ortholoc 3DI Midfoot/Flatfoot System, Wrightmedicaltechnologyinc (2012) Summary page 5.
- K152256: RECON system- Grubber Lapidus-, Platar Lapidus-, Tarsalis Plates and Screws, Normed Medizin-Technik GmbH (2015) Summary page 5.

## Most influential descendants
- K171510: Footmotion Plating System (2017), 1 descendant of its own
- K170843: Alians Fragment Specific (2017), 1 descendant of its own
- K221395: Footmotion Plating System (2022), 0 descendants of its own
- K213214: Xpert Wrist (2021), 0 descendants of its own
- K170012: Foot and Hand Motion (2017), 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/K161448
Methodology: https://510kreport.com/methodology