| Primary Device ID | B06214507124 | 
| NIH Device Record Key | 2cf8accb-4b5e-4ea3-82e0-1b62b2505939 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Aries-L Lateral Lumbar Interbody System | 
| Version Model Number | 1450-7124 | 
| Catalog Number | 1450-7124 | 
| 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 | B06214507124 [Primary] | 
| FZS | Curette, Surgical, General Use | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[B06214507124]
Moist Heat or Steam Sterilization
[B06214507124]
Moist Heat or Steam Sterilization
[B06214507124]
Moist Heat or Steam Sterilization
[B06214507124]
Moist Heat or Steam Sterilization
[B06214507124]
Moist Heat or Steam Sterilization
[B06214507124]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2022-06-10 | 
| Device Publish Date | 2020-05-12 | 
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