| Primary Device ID | 00721902170638 |
| NIH Device Record Key | 921fb657-486a-4302-a3d9-498700b96373 |
| Commercial Distribution Discontinuation | 2018-10-08 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | THREADED CR-Ti |
| Version Model Number | 6180206 |
| Company DUNS | 830350380 |
| Company Name | MEDTRONIC SOFAMOR DANEK, 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |