| Primary Device ID | 00190837081492 |
| NIH Device Record Key | e565db71-ae94-4710-9d64-f99f04e67656 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProLift Lateral |
| Version Model Number | 58-2660-0708 |
| Catalog Number | 58-2660-0708 |
| 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 | true |
| 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 |