# K241539: Activmotion S

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Jul 30, 2024 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: 14 generations back to K962616 (1996). 240 ancestors in all.
No later device cites it as a predicate yet.
0 of 241 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173746: Activmotion Range, Newclip Technics (2018) Summary page 5.
- K141796: Depuy Synthes Tomofix Osteotomy System, Synthes (USA) Products, LLC (2014) Summary page 5.
- K041601: Surfix Knee Osteotomy System, Surfix Technologies (2004) Summary page 5.

## Indications for use
The implants of the Activmotion range are indicated for knee osteotomy in adults.

Source page: https://510kreport.com/device/K241539
Methodology: https://510kreport.com/methodology