Klassic Knee Template, Tibial Baseplate, Revision

GUDID 00810094692674

Klassic Knee Template, Tibial Baseplate, Revision

TOTAL JOINT ORTHOPEDICS, INC.

Surgical implant template, reusable
Primary Device ID00810094692674
NIH Device Record Key9838a722-aec1-4880-b355-ed8ca6ce754d
Commercial Distribution StatusIn Commercial Distribution
Brand NameKlassic Knee Template, Tibial Baseplate, Revision
Version Model Number2909.00.000
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

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

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100810094692674 [Primary]

FDA Product Code

HWTTemplate

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-15
Device Publish Date2026-01-07

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00810094692766 - CR Femoral Trial, Grit Blasted2026-02-13 CR Femoral Trial, Grit Blasted, Size 5
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00810094692780 - CR Femoral Trial, Grit Blasted2026-02-13 CR Femoral Trial, Grit Blasted, Size 7
00810094692674 - Klassic Knee Template, Tibial Baseplate, Revision2026-01-15Klassic Knee Template, Tibial Baseplate, Revision
00810094692674 - Klassic Knee Template, Tibial Baseplate, Revision2026-01-15 Klassic Knee Template, Tibial Baseplate, Revision

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