Universal Cone Impactor Head, Size 7, 24°

GUDID 00810094692018

Cone Impactor Head, Size 7, 24 degrees

TOTAL JOINT ORTHOPEDICS, INC.

Orthopaedic implant impactor, reusable

Primary Device ID	00810094692018
NIH Device Record Key	70974684-a3e8-45fc-9a5f-dfb8b8e95a40
Commercial Distribution Status	In Commercial Distribution
Brand Name	Universal Cone Impactor Head, Size 7, 24°
Version Model Number	2021.07.024
Company DUNS	078416717
Company Name	TOTAL JOINT ORTHOPEDICS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com
Phone	8014866070
Email	kcardall@tjoinc.com

Device Dimensions

Device Size Text, specify	0
Device Size Text, specify	0
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Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810094692018 [Primary]

FDA Product Code

HWA

Impactor