Retropsoas Technologies, LLC
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242457 | EARP Interbody System | October 7, 2024 |
| K241917 | EARP Nerve Cuff Electrode | July 31, 2024 |