The following data is part of a premarket notification filed by Shandong Weigao Orthopaedic Device Co., Ltd with the FDA for Premier.
| Device ID | K160320 |
| 510k Number | K160320 |
| Device Name: | Premier |
| Classification | Orthosis, Spinal Pedicle Fixation |
| Applicant | Shandong Weigao Orthopaedic Device Co., Ltd No. 26 Xiangjiang Road, Tourist Resorts Weihai, CN 264203 |
| Contact | Han Wang |
| Correspondent | Diana Hong Mid-Link Consulting Co., Ltd P.O. Box 120-119 Shanghai, CN 200120 |
| Product Code | MNI |
| Subsequent Product Code | KWP |
| Subsequent Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-02-05 |
| Decision Date | 2016-04-01 |
| Summary: | summary |