| Primary Device ID | 00190837012786 | 
| NIH Device Record Key | 497c8282-023f-478f-91bf-c474b5cbc4d1 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Plateau-X Spacer System | 
| Version Model Number | 84-2250-709 | 
| Company DUNS | 183641617 | 
| Company Name | Life Spine, 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 | 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 |