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 |