| Primary Device ID | 00810017912353 |
| NIH Device Record Key | 62ee99c1-8281-43a1-858a-580dfa085d2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Inserter |
| Version Model Number | CI-INSERTER |
| Catalog Number | CI-INSERTER |
| Company DUNS | 085718404 |
| Company Name | ELEVATION SPINE, 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 | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |