| Primary Device ID | 00613994839251 |
| NIH Device Record Key | 3370c7bf-e3f9-4ae9-a598-86f8d30c4548 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vantage Anterior Fixation System |
| Version Model Number | X0410358 |
| 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 |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Outer Diameter | 9 Millimeter |
| Length | 20 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994839251 [Primary] |
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
[00613994839251]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-09 |
| 00613994839305 | BOLT X0410352 VAN TI 8X35 |
| 00613994839299 | BOLT X0410353 VAN TI 8X40 |
| 00613994839282 | BOLT X0410354 VAN TI 8X45 |
| 00613994839275 | BOLT X0410355 VAN TI 8X50 |
| 00613994839268 | BOLT X0410356 VAN TI 8X55 |
| 00613994839251 | BOLT X0410358 VAN TI 9X20 |
| 00613994839244 | BOLT X0410359 VAN TI 9X25 |
| 00613994839237 | BOLT X0410360 VAN TI 9X30 |
| 00613994839220 | BOLT X0410361 VAN TI 9X35 |
| 00613994839213 | BOLT X0410362 VAN TI 9X40 |
| 00613994839206 | BOLT X0410363 VAN TI 9X45 |
| 00613994839190 | BOLT X0410364 VAN TI 9X50 |
| 00613994839183 | BOLT X0410365 VAN TI 9X55 |