| Primary Device ID | B707128320050010 |
| NIH Device Record Key | f39904f0-df87-4532-95a5-b4a0e1cb3015 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KIT DUALX LLIF 7-9MM x 0 DEG x 40MM |
| Version Model Number | 12832005001 |
| 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 |