| Primary Device ID | 00819475010793 |
| NIH Device Record Key | 25be54b8-2461-43c3-a961-44988614d48d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InterFuse L |
| Version Model Number | 9119-08-21-50-8 |
| Catalog Number | 9119-08-21-50-8 |
| Company DUNS | 362264421 |
| Company Name | VERTEBRAL TECHNOLOGIES, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com | |
| Phone | 952-912-5400 |
| CustomerService@vti-spine.com |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Height | 8 Millimeter |
| Width | 21 Millimeter |
| Length | 50 Millimeter |
| Angle | 8 degree |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient temperatures in a clean dry area |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00819475010793 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-06-10 |
| 00819475010922 | Intervertebral Body Fusion Device |
| 00819475010915 | Intervertebral Body Fusion Device |
| 00819475010908 | Intervertebral Body Fusion Device |
| 00819475010892 | Intervertebral Body Fusion Device |
| 00819475010885 | Intervertebral Body Fusion Device |
| 00819475010878 | Intervertebral Body Fusion Device |
| 00819475010861 | Intervertebral Body Fusion Device |
| 00819475010854 | Intervertebral Body Fusion Device |
| 00819475010847 | Intervertebral Body Fusion Device |
| 00819475010830 | Intervertebral Body Fusion Device |
| 00819475010823 | Intervertebral Body Fusion Device |
| 00819475010816 | Intervertebral Body Fusion Device |
| 00819475010809 | Intervertebral Body Fusion Device |
| 00819475010793 | Intervertebral Body Fusion Device |
| 00819475010786 | Intervertebral Body Fusion Device |
| 00819475010779 | Intervertebral Body Fusion Device |
| 00819475010762 | Intervertebral Body Fusion Device |
| 00819475010755 | Intervertebral Body Fusion Device |
| 00819475010748 | Intervertebral Body Fusion Device |
| 00819475010731 | Intervertebral Body Fusion Device |
| 00819475010724 | Intervertebral Body Fusion Device |
| 00819475010717 | Intervertebral Body Fusion Device |
| 00819475010700 | Intervertebral Body Fusion Device |
| 00819475010694 | Intervertebral Body Fusion Device |
| 00819475010687 | Intervertebral Body Fusion Device |
| 00819475010670 | Intervertebral Body Fusion Device |
| 00819475010663 | Intervertebral Body Fusion Device |
| 00819475010656 | Intervertebral Body Fusion Device |
| 00819475010649 | Intervertebral Body Fusion Device |
| 00819475010632 | Intervertebral Body Fusion Device |
| 00819475010625 | Intervertebral Body Fusion Device |
| 00819475010618 | Intervertebral Body Fusion Device |