Industrias Medicas Sampedro S.A.S
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K203282 | TECHFIT Patient-Specific Maxillofacial System | May 19, 2021 |
| K191641 | AFFINITY Variable Angle Distal Radius System, AFFINITY Variable Angle Distal Radius Plates, AFFI | September 16, 2019 |