Osteomed Implantes, Ltda
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K151553 | Anterior Cervical Plate System | February 10, 2016 |
| K143572 | Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DI | June 10, 2015 |
| K150294 | DPZ Pedicular Fixation System | June 5, 2015 |