Aesculap Implants Systems, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K231769 | activL® Next Generation Instrumentation | July 13, 2023 |
| K172235 | CoreHip® System | March 28, 2018 |
| K172032 | Modulift Vertebral Body Replacement (VBR) System | November 20, 2017 |
| K143443 | VEGA Knee System, Columbus Total Knee System | March 25, 2015 |