Primary Device ID | 00843210131122 |
NIH Device Record Key | 1f351dab-ef38-4565-8457-fa30fae27b3f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Altus Spine Cervical Interbody Fusion System |
Version Model Number | 210-3006 |
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 |