# K141548: High Tibial Osteotomy System

- Pathway: 510(k) (Traditional)
- Applicant: Newclip Technics
- Decided: Jan 30, 2015 after 233 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: 4 generations back to K000684 (2000). 17 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032187: Anthrex Titanium Opening Wedge Osteotomy System, Arthrex, Inc. (2003) Summary page 4.
- K041601: Surfix Knee Osteotomy System, Surfix Technologies (2004) Summary page 4.
- K063095: Humerus Locking Plating System, Newclip Technics (2006) Summary page 4.

## Most influential descendants
- K173746: Activmotion Range (2018), 1 descendant of its own
- K241539: Activmotion S (2024), 0 descendants of its own
- K213214: Xpert Wrist (2021), 0 descendants of its own

## Indications for use
The High Tibial Osteotomy System is indicated for fixation of high tibial osteotomy.

Source page: https://510kreport.com/device/K141548
Methodology: https://510kreport.com/methodology