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 |