| Primary Device ID | 00819475010359 |
| NIH Device Record Key | 310064f3-c340-48c6-8507-d4013cf8c7db |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InterFuse T |
| Version Model Number | 9091-08-20-10-Q |
| Catalog Number | 9091-08-20-10-Q |
| 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 | 10 degree |
| Angle | 10 degree |
| Angle | 10 degree |
| Angle | 10 degree |
| Angle | 10 degree |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 degree |
| Height | 8 Millimeter |
| Length | 20 Millimeter |
| Angle | 10 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 | 00819475010359 [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 | 3 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2015-09-15 |
| 00819475010984 | Intervertebral Body Fusion Device |
| 00819475010977 | Intervertebral Body Fusion Device |
| 00819475010601 | Intervertebral Body Fusion Device |
| 00819475010595 | Intervertebral Body Fusion Device |
| 00819475010588 | Intervertebral Body Fusion Device |
| 00819475010571 | Intervertebral Body Fusion Device |
| 00819475010564 | Intervertebral Body Fusion Device |
| 00819475010557 | Intervertebral Body Fusion Device |
| 00819475010540 | Intervertebral Body Fusion Device |
| 00819475010533 | Intervertebral Body Fusion Device |
| 00819475010526 | Intervertebral Body Fusion Device |
| 00819475010519 | Intervertebral Body Fusion Device |
| 00819475010502 | Intervertebral Body Fusion Device |
| 00819475010496 | Intervertebral Body Fusion Device |
| 00819475010489 | Intervertebral Body Fusion Device |
| 00819475010472 | Intervertebral Body Fusion Device |
| 00819475010465 | Intervertebral Body Fusion Device |
| 00819475010458 | Intervertebral Body Fusion Device |
| 00819475010403 | Intervertebral Body Fusion Device |
| 00819475010397 | Intervertebral Body Fusion Device |
| 00819475010380 | Intervertebral Body Fusion Device |
| 00819475010373 | Intervertebral Body Fusion Device |
| 00819475010366 | Intervertebral Body Fusion Device |
| 00819475010359 | Intervertebral Body Fusion Device |
| 00819475010342 | Intervertebral Body Fusion Device |
| 00819475010335 | Intervertebral Body Fusion Device |
| 00819475010328 | Intervertebral Body Fusion Device |
| 00819475010311 | Intervertebral Body Fusion Device |
| 00819475010304 | Intervertebral Body Fusion Device |
| 00819475010298 | Intervertebral Body Fusion Device |
| 00819475010281 | Intervertebral Body Fusion Device |
| 00819475010274 | Intervertebral Body Fusion Device |