GZC01A07C

GUDID 00840085214394

LLIF IMPLANT TRIAL, MODULAR, STRAIGHT

HYHTE HOLDINGS, INC.

Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial Spinal implant trial
Primary Device ID00840085214394
NIH Device Record Key83834321-97a8-45e5-b47e-a329b48206f7
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberGZC01A07C
Catalog NumberGZC01A07C
Company DUNS073029645
Company NameHYHTE HOLDINGS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM

Device Dimensions

Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree
Width18 Millimeter
Height7 Millimeter
Angle12 degree

Device Identifiers

Device Issuing AgencyDevice ID
GS100840085214394 [Primary]

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


[00840085214394]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-22
Device Publish Date2021-07-14

Devices Manufactured by HYHTE HOLDINGS, INC.

00840085265167 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265174 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265181 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265198 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265204 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265211 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265228 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265235 - NA2024-04-22 CORTICAL CANCELLOUS CANNULATED SCREW

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.