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 |