Primary Device ID | 00814216023681 |
NIH Device Record Key | 06ca6c01-6483-4a85-a3a0-7c43e0f993bd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FortiCore PLIF |
Version Model Number | 10492-2207 |
Catalog Number | 10492-2207 |
Company DUNS | 079898044 |
Company Name | NANOVIS 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 | 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 |