Universal Cone Trial, Size 4, 18°

GUDID 00810094692056

Cone Trial, Size 4, 18 degrees

TOTAL JOINT ORTHOPEDICS, INC.

Knee femur prosthesis trial, reusable
Primary Device ID00810094692056
NIH Device Record Keyc854ac65-898e-4ebc-8631-982da4bd7a92
Commercial Distribution StatusIn Commercial Distribution
Brand NameUniversal Cone Trial, Size 4, 18°
Version Model Number2022.04.018
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

Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@tjoinc.com
Phone8014866070
Emailkcardall@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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100810094692056 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


[00810094692056]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-09-12
Device Publish Date2024-09-04

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