MicroPort NeuroTech (Shanghai) Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242154 | Numen Coil Embolization System; NumenFR Detachment System | September 30, 2024 |
| K232955 | Numen Coil Embolization System; NumenFR Detachment System | January 10, 2024 |
| K203625 | Numen Coil Embolization System; NumenFR Detachment System | September 1, 2021 |