Posterior Femoral Augment Trial

GUDID 00810094691684

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

TOTAL JOINT ORTHOPEDICS, INC.

Knee femur prosthesis trial, reusable

Primary Device ID	00810094691684
NIH Device Record Key	ada5cf5a-8ff8-44b9-a82a-028b4c1765c0
Commercial Distribution Status	In Commercial Distribution
Brand Name	Posterior Femoral Augment Trial
Version Model Number	2809.05.005
Company DUNS	078416717
Company Name	TOTAL JOINT ORTHOPEDICS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com
Phone	801-486-6070
Email	udi@tjoinc.com

Device Dimensions

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Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810094691684 [Primary]

FDA Product Code

LXH	Orthopedic Manual Surgical Instrument