Primary Device ID | B167S11000001220 |
NIH Device Record Key | 2c2e8cde-5a9d-44f6-b7aa-94941aedb419 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CURE 2.0™ ACP |
Version Model Number | S1-10-00001-22 |
Company DUNS | 182698477 |
Company Name | MEDITECH 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |