| Primary Device ID | W4184048010T0479 |
| NIH Device Record Key | ecef9841-462b-41e7-8ac9-4f6f90ce51f9 |
| Commercial Distribution Discontinuation | 2019-06-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | DBX® |
| Version Model Number | 048010 |
| Catalog Number | 048010 |
| Company DUNS | 187560545 |
| Company Name | Musculoskeletal Transplant Foundation, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | true |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |