Primary Device ID | 00190837013127 |
NIH Device Record Key | 5c99cd1d-6a1e-4dec-8dbc-0281c70dd212 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Presidio Anterior Lumbar Fixation System |
Version Model Number | 125-10-36 |
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 |