Primary Device ID | 00190837083458 |
NIH Device Record Key | f517d5c5-da79-4040-9ddf-2cbabc2a42e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Plateau A |
Version Model Number | 126-230 |
Catalog Number | 126-230 |
Company DUNS | 183641617 |
Company Name | Life 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 | 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 |