| Primary Device ID | 00849777011693 |
| NIH Device Record Key | dbc96148-9a1d-4ada-bbad-05a153093870 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VIA DBM Putty, 10cc |
| Version Model Number | DBM010 |
| Company DUNS | 081224143 |
| Company Name | Xtant Medical Holdings, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| 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 |
| 00840311207435 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x25 |
| 00840311207442 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x30 |
| 00840311207459 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x35 |
| 00840311207466 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x40 |
| 00840311207473 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x45 |
| 00840311207480 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x50 |
| 00840311207497 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x55 |
| 00840311207503 - Cortera Spinal Fixation System | 2024-10-17 Rod, Ti, Prebent, 6.0x60 |