| Primary Device ID | 00190837044602 |
| NIH Device Record Key | 3743add0-3069-493b-a5d2-bd3fe768726e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aileron Posterior Fusion System |
| Version Model Number | 2015-0070 |
| Catalog Number | 2015-0070 |
| Company DUNS | 183641617 |
| Company Name | Life 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |