The following data is part of a premarket notification filed by Suzhou Kangli Orthopaedics Instrument Co., Ltd with the FDA for Kangli Pedical Screw Spinal System.
| Device ID | K142290 |
| 510k Number | K142290 |
| Device Name: | KangLi Pedical Screw Spinal System |
| Classification | Orthosis, Spondylolisthesis Spinal Fixation |
| Applicant | SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD SHA ZHOU EAST ROAD Zhangjiagang City, CN 215625 |
| Contact | Jin Hua Huang |
| Correspondent | Alice Gong Shanghai Yarui Consultant Co., Ltd 503 Room 8, Building, 600 Liu Zhou Road Shanghai, CN 200233 |
| Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-08-18 |
| Decision Date | 2014-11-24 |
| Summary: | summary |