| Primary Device ID | 09348215129019 |
| NIH Device Record Key | 354b48db-8032-4651-a9e9-bd37ef8e7183 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Verteloc Spinal System |
| Version Model Number | 131-14-1505 |
| Company DUNS | 751993028 |
| Company Name | SIGNATURE ORTHOPAEDICS PTY LTD |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 09348215129019 [Primary] |
| PLR | Spinal Vertebral Body Replacement Device - Cervical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-12 |
| Device Publish Date | 2024-03-04 |
| 09348215129132 | 131-14-0040 |
| 09348215129125 | 131-14-0030 |
| 09348215129118 | 131-14-0020 |
| 09348215129101 | 131-14-0010 |
| 09348215129095 | 131-14-0008 |
| 09348215129088 | 131-14-1713 |
| 09348215129071 | 131-14-1711 |
| 09348215129064 | 131-14-1709 |
| 09348215129057 | 131-14-1705 |
| 09348215129040 | 131-14-1513 |
| 09348215129033 | 131-14-1511 |
| 09348215129026 | 131-14-1509 |
| 09348215129019 | 131-14-1505 |
| 09348215129002 | 131-14-1013 |
| 09348215128999 | 131-14-1011 |
| 09348215128982 | 131-14-1009 |
| 09348215128975 | 131-14-1005 |