| Primary Device ID | W4184420800T0473 |
| NIH Device Record Key | 98a3c353-d1fc-4693-819d-b4d492a13dfc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Legacy DBM |
| Version Model Number | 420800 |
| Catalog Number | 420800 |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |