GZC10B10A

GUDID 00840085210280

LLIF IMPLANT TRIAL, MODULAR, ANGLED LEFT

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 ID00840085210280
NIH Device Record Keye955d1e7-c681-4633-b4b2-38a3bafc4282
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberGZC10B10A
Catalog NumberGZC10B10A
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

Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree
Width20 Millimeter
Height10 Millimeter
Angle0 degree

Device Identifiers

Device Issuing AgencyDevice ID
GS100840085210280 [Primary]

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

Moist Heat or Steam Sterilization


[00840085210280]

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.

00840085265105 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265112 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265129 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265136 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265143 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085265150 - NA2024-04-19 CORTICAL CANCELLOUS CANNULATED SCREW
00840085257469 - NA2024-04-18 DUAL LEAD SCREW
00840085257476 - NA2024-04-18 DUAL LEAD SCREW

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