| Primary Device ID | 90850470007008 |
| NIH Device Record Key | 749fa285-2f7e-4884-9e26-2c8090d48f8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ARTAS System |
| Version Model Number | Cart |
| Catalog Number | FP-40000 |
| Company DUNS | 627212587 |
| Company Name | RESTORATION ROBOTICS, 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |