Primary Device ID | 00840019929233 |
NIH Device Record Key | ff04ff83-e433-4d84-a8b0-18b265a9d75a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ShurFit ACIF Titanium |
Version Model Number | CRT006 |
Catalog Number | CRT006 |
Company DUNS | 079398589 |
Company Name | PRECISION SPINE, INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
Lot Batch | false |
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 |