| Primary Device ID | B06211503000 |
| NIH Device Record Key | 556c3225-4735-418d-98a0-176fe7abd641 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Aries-T Lumbar Interbody System |
| Version Model Number | 1150-3000 |
| Catalog Number | 1150-3000 |
| Company DUNS | 933442068 |
| Company Name | Osseus Fusion Systems, 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B06211503000 [Primary] |
| FZX | Guide, Surgical, Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
[B06211503000]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-21 |
| Device Publish Date | 2020-05-13 |
| B06211507110 | 10" Bone Funnel Impactor |
| B06211503000 | Aries TSLIF Inserter |