| Primary Device ID | B114210060 |
| NIH Device Record Key | 39c7491f-64fd-401b-9da9-2f9a9a67e04e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cervical Interbody Spacer Trial |
| Version Model Number | 6mm Trial |
| Catalog Number | 210-06 |
| Company DUNS | 832116532 |
| Company Name | CALVARY SPINE, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 |
| B114211090 | Dual Head Trial for 9mm standard and large cervical inter-vertebral body spacers |
| B114211080 | Dual Head Trial for 8mm standard and large cervical inter-vertebral body spacers |
| B114211070 | Dual Head Trial for 7mm standard and large cervical inter-vertebral body spacers |
| B114211060 | Dual Head Trial for 6mm standard and large cervical inter-vertebral body spacers |
| B114211050 | Dual Head Trial for 5mm standard and large cervical inter-vertebral body spacers |
| B114210090 | Trial for 9mm standard cervical inter-vertebral body spacer |
| B114210080 | Trial for 8mm standard cervical inter-vertebral body spacer |
| B114210070 | Trial for 7mm standard cervical inter-vertebral body spacer |
| B114210060 | Trial for 6mm standard cervical inter-vertebral body spacer |
| B114210050 | Trial for 5mm standard cervical inter-vertebral body spacer |