| Primary Device ID | 00190837031367 |
| NIH Device Record Key | d633c9ed-6881-44dc-bb5d-31e89adb5be7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nautilus Non-Cannulated Iliac |
| Version Model Number | 485-110-5 |
| Catalog Number | 485-110-5 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00190837031367 [Primary] |
| NKB | Thoracolumbosacral pedicle screw system |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
[00190837031367]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-15 |
| Device Publish Date | 2019-11-07 |
| 00190837031367 | 485-110-5 |
| 00190837031350 | 485-105-5 |
| 00190837031343 | 485-100-5 |
| 00190837031336 | 485-95-5 |
| 00190837031329 | 475-110-5 |
| 00190837031312 | 475-105-5 |
| 00190837031305 | 475-100-5 |
| 00190837031299 | 475-95-5 |