Primary Device ID | 00190837015800 |
NIH Device Record Key | 1ca727f5-99a2-4b41-9995-ff3960d64d9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Plateau-X Spacer System |
Version Model Number | 89-1850-014 |
Company DUNS | 183641617 |
Company Name | Life 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 | 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 |