The following data is part of a premarket notification filed by Shandong Weigao Orthopaedic Device Co., Ltd. with the FDA for Premier.
Device ID | K170861 |
510k Number | K170861 |
Device Name: | Premier |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Shandong Weigao Orthopaedic Device Co., Ltd. No. 26 Xiangjiang Road, Tourist Resorts Weihai, CN 264203 |
Contact | Han Wang |
Correspondent | Justin Eggleton Musculoskeletal Clinical Regulatory Advisers, LLC 1050 K Street NW, Suite 1000 Washington, DC 20001 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-23 |
Decision Date | 2017-08-04 |
Summary: | summary |