TDHB20500

GUDID 00840085274053

ENDPLATE, 20MM, VARIABLE LORDISIS, LATERAL, ZERO, L.

HYHTE HOLDINGS, INC.

Metallic spinal interbody fusion cage
Primary Device ID00840085274053
NIH Device Record Key505453db-4d7c-4889-aba5-4bbb19965e63
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberTDHB20500
Catalog NumberTDHB20500
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
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM
Phone7608148047
EmailTROY@ASTURAMEDICAL.COM

Device Dimensions

Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter
Height50 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100840085274053 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


[00840085274053]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-11-06
Device Publish Date2024-10-29

Devices Manufactured by HYHTE HOLDINGS, INC.

00840085272509 - NA2024-11-06 ENDPLATE, 20MM, VARIABLE LORDISIS, LATERAL, FULL, R.
00840085273322 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273339 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273346 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273353 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273360 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273377 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.
00840085273384 - NA2024-11-06 ENDPLATE, 16MM, VARIABLE LORDOSIS, LATERAL, FULL, L.

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