Primary Device ID | 00190837057329 |
NIH Device Record Key | 2a7d1bf6-a99f-43e0-8249-8752f298a4b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nautilus Spinal System |
Version Model Number | 385-65-5 |
Catalog Number | 385-65-5 |
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 | 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 |