| Primary Device ID | W4184420802T0473 |
| NIH Device Record Key | bf8d8beb-8b55-44db-9756-6063a288f98d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Legacy DBM |
| Version Model Number | 420802 |
| Catalog Number | 420802 |
| 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 |