Shanghai Reach Medical Instrument 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 |
|---|
| K232069 | Expandable Lumbar Fusion Cage (Type I,Type II) | November 29, 2023 |
| K221745 | Sterile Posterior Spinal Fixation System | August 31, 2022 |
| K201737 | Posterior Spinal Fixation System | June 21, 2021 |