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 |