PS-Post Box Trial, Klassic ONE

GUDID 00819251026468

PS-Post Box Trial, Size 5

TOTAL JOINT ORTHOPEDICS, INC.

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Primary Device ID00819251026468
NIH Device Record Key793bf3e7-d3dc-4921-9eaf-b51f4e681614
Commercial Distribution StatusIn Commercial Distribution
Brand NamePS-Post Box Trial, Klassic ONE
Version Model Number2165.05.000
Company DUNS078416717
Company NameTOTAL JOINT ORTHOPEDICS, 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 Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com

Device Dimensions

Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100819251026468 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


[00819251026468]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-19
Device Publish Date2020-10-09

On-Brand Devices [PS-Post Box Trial, Klassic ONE ]

00819251026482PS-Post Box Trial, Size 7
00819251026475PS-Post Box Trial, Size 6
00819251026468PS-Post Box Trial, Size 5
00819251026451PS-Post Box Trial, Size 4
00819251026444PS-Post Box Trial, Size 3
00819251026437PS-Post Box Trial, Size 2
00819251026420PS-Post Box Trial, Size 1
00819251029384PS-Post Box Trial, Size 7
00819251029377PS-Post Box Trial, Size 6
00819251029360PS-Post Box Trial, Size 5
00819251029353PS-Post Box Trial, Size 4
00819251029346PS-Post Box Trial, Size 3
00819251029339PS-Post Box Trial, Size 2
00819251029322PS-Post Box Trial, Size 1

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