# K173746: Activmotion Range

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Feb 27, 2018 after 81 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: 13 generations back to K962616 (1996). 239 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 241 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141796: Depuy Synthes Tomofix Osteotomy System, Synthes (USA) Products, LLC (2014) Summary page 4.
- K141548: High Tibial Osteotomy System, Newclip Technics (2015) Summary page 4.
- K163361: ANTHEM™ Fracture System, Globus Medical, Inc. (2017) Summary page 4.

## Most influential descendants
- K241539: Activmotion S (2024), 0 descendants of its own

## Indications for use
The Activmotion range is intended for knee osteotomy in adults.

Source page: https://510kreport.com/device/K173746
Methodology: https://510kreport.com/methodology