BA103009B

GUDID 00841379100355

TLIF SPACER

HYHTE HOLDINGS, INC.

Polymeric spinal interbody fusion cage
Primary Device ID00841379100355
NIH Device Record Keyb7a61976-1743-4364-a2c9-fe426ed8af48
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberBA103009B
Catalog NumberBA103009B
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

Device Dimensions

Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter
Angle5 degree
Height9 Millimeter
Length30 Millimeter
Width10 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379100355 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


[00841379100355]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-02-24
Device Publish Date2016-09-09

Devices Manufactured by HYHTE HOLDINGS, INC.

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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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