ACAB55030

GUDID 00841379131502

ROD, STRAIGHT

HYHTE HOLDINGS, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00841379131502
NIH Device Record Key130eb7cb-1530-45bd-8e42-874779d69c1f
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberACAB55030
Catalog NumberACAB55030
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
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

Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter
Length30 Millimeter
Outer Diameter5.5 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379131502 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MNHOrthosis, Spondylolisthesis Spinal Fixation

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


[00841379131502]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

Devices Manufactured by HYHTE HOLDINGS, INC.

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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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