# K142290: KangLi pedical screw spinal system

- Pathway: 510(k) (Traditional)
- Applicant: Suzhou Kangli Orthopaedics Instrument Co., Ltd.
- Decided: Nov 24, 2014 after 98 days
- Product code: MNH (Orthosis, Spondylolisthesis Spinal Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3070
- 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 K031655 (2003). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140053: Kangli Pedicle Screw Spinal System, Suzhou Kangli Orthopaedics Instrument Co., Ltd. (2014) Summary page 4.

## Indications for use
KangLi® pedicle screw spinal system is intended for posterior, non-cervical, pedicle fixation for the following indications: severe spondylolisthesis (grade 3 or 4) of the L5-SI vertebrae; trauma (i.e. fracture or dislocation), spinal stenosis, curvatures (i.e. scoliosis, kyphosis, and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion. The device is to be used in skeletally mature patients, and for stabilization and immobilization of the spine as an adjunct to fusion with bone graft. The levels of fixation are T8 — S1.

Source page: https://510kreport.com/device/K142290
Methodology: https://510kreport.com/methodology