Primary Device ID | 00840085248603 |
NIH Device Record Key | ea486bc2-6a43-4d71-8440-1d246a569ed6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | KJB13000B |
Catalog Number | KJB13000B |
Company DUNS | 073029645 |
Company Name | HYHTE HOLDINGS, 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 |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM | |
Phone | 7608148047 |
PARKER@ASTURAMEDICAL.COM |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Height | 13 Millimeter |
Angle | 15 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840085248603 [Primary] |
OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
[00840085248603]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-16 |
Device Publish Date | 2022-05-06 |
00840085257469 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257476 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257483 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257490 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257506 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257513 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257520 - NA | 2024-04-18 DUAL LEAD SCREW |
00840085257537 - NA | 2024-04-18 DUAL LEAD SCREW |