FAGA50028

GUDID 00841379143406

POLYAXIAL SCREW #1, SMOOTH SHANK

HYHTE HOLDINGS, INC.

Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable
Primary Device ID00841379143406
NIH Device Record Key87ba7677-5365-4ac2-bd61-13a5d2127b49
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberFAGA50028
Catalog NumberFAGA50028
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
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
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM
Phone7608148047
EmailPARKER@ASTURAMEDICAL.COM

Device Dimensions

Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter
Width5 Millimeter
Length28 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841379143406 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKGPosterior Cervical Screw System

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


[00841379143406]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-27
Device Publish Date2021-07-19

Devices Manufactured by HYHTE HOLDINGS, INC.

00840085254413 - NA2024-05-07 POLYAXIAL, TULIP
00840085254420 - NA2024-05-07 POLYAXIAL, HIGH TOP, TULIP
00840085254437 - NA2024-05-07 POLYAXIAL, EXTENDED TAB, TULIP
00840085254444 - NA2024-05-07 FAVORED ANGLE M/L, TULIP
00840085254451 - NA2024-05-07 FAVORED ANGLE M/L, HIGH TOP, TULIP
00840085254468 - NA2024-05-07 FAVORED ANGLE M/L, EXTENED TAB, TULIP
00840085254475 - NA2024-05-07 FAVORED ANGLE C/C, TULIP
00840085254482 - NA2024-05-07 FAVORED ANGLE C/C, HIGH TOP, TULIP

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