# K133840: Kangli Locking Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Suzhou Kangli Orthopaedics Instrument Co., Ltd.
- Decided: Jul 29, 2014 after 223 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: 8 generations back to K981372 (1998). 17 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130340: Locking Bone Plates and Screws, Weigao Orthopaedic Device Co., Ltd. (2013) Summary page 1.

## Most influential descendants
- K150009: Baide (2015), 1 descendant of its own
- K240958: Locking Plates and Screws Systems (2025), 0 descendants of its own

## Indications for use
KangLi® locking plate system is intended for adult patients as indicated for fixation of fractures of tibia.

Source page: https://510kreport.com/device/K133840
Methodology: https://510kreport.com/methodology