| Primary Device ID | B707125330060050 |
| NIH Device Record Key | 9620046a-e9ed-4492-ad4d-a2d046224b2f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KIT DUALX TLIF 8 DEG x 9-12MM |
| Version Model Number | 12533006005 |
| Company DUNS | 081021000 |
| Company Name | AMPLIFY SURGICAL, 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |