Primary Device ID | 09348215129101 |
NIH Device Record Key | 89d33d99-18da-4cbf-a3b9-ae11beb3e886 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Verteloc Spinal System |
Version Model Number | 131-14-0010 |
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 | 09348215129101 [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 |