Revision Modular Tibial Broach

GUDID 00810094692537

Revision Modular Tibial Broach, Sz 5

TOTAL JOINT ORTHOPEDICS, INC.

Orthopaedic broach
Primary Device ID00810094692537
NIH Device Record Keyd246e432-f090-4a29-b4c9-772759ba1d00
Commercial Distribution StatusIn Commercial Distribution
Brand NameRevision Modular Tibial Broach
Version Model Number2905.05.000
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 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
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com
Phone801-486-6070
Emailbsiddoway@tjoinc.com

Device Dimensions

Device Size Text, specify0
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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100810094692537 [Primary]

FDA Product Code

HTQBroach

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


[00810094692537]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-05-22
Device Publish Date2025-05-14

On-Brand Devices [Revision Modular Tibial Broach]

00810094692537Revision Modular Tibial Broach, Sz 5
00810094692520Revision Modular Tibial Broach, Sz 3
00810094692513Revision Modular Tibial Broach, Sz 1

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