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 |