Shanghai Sanyou Medical Co, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K230872 | Halis Lumbar Cage System, Lydia Anterior Lumbar Fusion System, Dica Direction Changeable Lumbar C | December 12, 2023 |
| K230961 | Zeus Spinal System | October 10, 2023 |
| K231931 | Adena-Zina Spinal System | July 28, 2023 |
| K211689 | KEYSTONE PEEK Cage System | September 21, 2021 |
| K212066 | Adena-Zina System | August 16, 2021 |
| K163366 | Shanghai Sanyou CARMEN Cervical Fusion System | October 5, 2017 |
| K163422 | Shanghai Sanyou PEEK Cage System | September 18, 2017 |
| K152781 | Adena-Zina System | February 12, 2016 |
| K131512 | KATIA SYSTEM | August 7, 2013 |