| Primary Device ID | 03663422070005 |
| NIH Device Record Key | 60bfe12e-05c0-4367-b455-603332dc4a8a |
| Commercial Distribution Discontinuation | 2024-05-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Ayers Rock Cervical interbody fusion system |
| Version Model Number | 2 |
| Catalog Number | AR2C51213 |
| Company DUNS | 281075270 |
| Company Name | SPINEWAY |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |
| Width | 13 Millimeter |
| Length | 12 Millimeter |
| Height | 5 Millimeter |
| Device Size Text, specify | 0 |