Primary Device ID | M739PO30130 |
NIH Device Record Key | 2cd0d515-43aa-4bdc-8be0-7fbe7dd05e5e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TLIF Curved-O, 30 x 13mm |
Version Model Number | PO3013 |
Company DUNS | 836975784 |
Company Name | CAPTIVA SPINE, INC. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |