Kico Knee Innovation Company Pty, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243950 | ARVIS® Shoulder | January 13, 2025 |
| K242009 | 360CAS Knee | August 8, 2024 |