Posterior Femoral Augment Trial

GUDID 00810094691691

Posterior Femoral Augment Trial Size 5-6-7, 10mm

TOTAL JOINT ORTHOPEDICS, INC.

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Primary Device ID00810094691691
NIH Device Record Key1e1770ca-c9ee-44b7-9d2a-6637112d84ce
Commercial Distribution StatusIn Commercial Distribution
Brand NamePosterior Femoral Augment Trial
Version Model Number2809.05.010
Company DUNS078416717
Company NameTOTAL JOINT ORTHOPEDICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
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

Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com
Phone801-486-6070
Emailudi@tjoinc.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic Knee System should be stored in a clean, dry location at room temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS100810094691691 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


[00810094691691]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-11
Device Publish Date2024-06-03

On-Brand Devices [Posterior Femoral Augment Trial]

00810094691691Posterior Femoral Augment Trial Size 5-6-7, 10mm
00810094691684Posterior Femoral Augment Trial Size 5-6-7, 5mm
00810094691677Posterior Femoral Augment Trial Size 3-4, 10mm
00810094691660Posterior Femoral Augment Trial Size 3-4, 5mm
00810094691653Posterior Femoral Augment Trial Size 1-2, 10mm
00810094691646Posterior Femoral Augment Trial Size 1-2, 5mm

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