# K080992: Aesculap Implant Systems High Tibial Osteotomy Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Aesculap Implant Systems, Inc.
- Decided: Sep 4, 2008 after 150 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: 1 generation back to K973812 (1998). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K973812: Arthrex Puddu Osteotomy System, Arthrex, Inc. (1998) Summary page 1.

## Most influential descendants
- K102505: Hto Plating System (2010), 0 descendants of its own

## Indications for use
The Aesculap Implant Systems High Tibial Osteotomy (HTO) Plating System is intended to be used in conjunction with bone screws to provide fixation following Proximal Tibial opening wedge osteotomies.

Source page: https://510kreport.com/device/K080992
Methodology: https://510kreport.com/methodology