Foundation Surgical Group, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K241468 | Vertiwedge® Intraosseous System | November 7, 2024 |
| K241487 | Interwedge® Standalone Lateral | October 2, 2024 |