Celestray Biotech Company, LLC.,
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2024-01-29
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K230794 | Rebuilder Nerve Guidance Conduit | JXI | 2024-01-29 | View |
| 510(k) | K222220 | SpinMedix Absorbable Fibrous Membrane | OWW | 2023-07-06 | View |
No matching devices.