| Primary Device ID | 00843210130651 |
| NIH Device Record Key | 46db8876-75a0-4810-808b-01bb65792ec4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Altus Spine Interbody Fusion System |
| Version Model Number | 1000-2616 |
| Company DUNS | 078331322 |
| Company Name | Altus Spine, LLC |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com | |
| Phone | +1(610)355-4156 |
| Info@altus-spine.com |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Height | 16 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00843210130651 [Primary] |
| MAX | Intervertebral fusion device with bone graft, lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
[00843210130651]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2018-09-25 |