The following data is part of a premarket notification filed by Jiangsu Baide Medical Intrument Co.,ltd. with the FDA for Baide.
Device ID | K150009 |
510k Number | K150009 |
Device Name: | Baide |
Classification | Plate, Fixation, Bone |
Applicant | Jiangsu Baide Medical Intrument Co.,Ltd. South Side Of Dongqi Road Zhangjiagang City, CN 215627 |
Contact | Mr.kang Shui |
Correspondent | Alice Gong Shanghai Yarui Consultant Co., Ltd 503 Room 8, Building, 600 Liu Zhou Road Shanghai, CN 200233 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-01-02 |
Decision Date | 2015-02-25 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BAIDE 87266304 5308597 Live/Registered |
shenzhen shi baide brothers technology co.,LTD 2016-12-13 |