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Matrix Surgical Holdings, LLC/Matrix Surgical USA
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K180249 | OmniPore DUROMAX Surgical Implants | October 11, 2018 |
| K133046 | OMNIPORE CUSTOMIZED SURGICAL IMPLANTS | May 14, 2014 |