The following data is part of a premarket notification filed by Suzhou Kangli Orthopaedics Instrument Co., Ltd with the FDA for Kangli Pedicle Screw Spinal System.
Device ID | K140053 |
510k Number | K140053 |
Device Name: | KANGLI PEDICLE SCREW SPINAL SYSTEM |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT CO., LTD 503 ROOM, 8 BUILDING, 600 LIU ZHOU ROAD Shanghai, CN 200233 |
Contact | Alice Gong |
Correspondent | Alice Gong SUZHOU KANGLI ORTHOPAEDICS INSTRUMENT 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 | 2014-01-09 |
Decision Date | 2014-06-26 |
Summary: | summary |