| Primary Device ID | 00190837016074 | 
| NIH Device Record Key | d8d07e08-2002-4746-94ac-72e02c8c2d14 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Plateau-X Spacer System | 
| Version Model Number | 89-2240-008 | 
| Company DUNS | 183641617 | 
| Company Name | Life Spine, Inc. | 
| Device Count | 1 | 
| DM Exempt | true | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| 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 |