Klassic HD Hip System Offset Femoral Stem, Porous, size 7

GUDID 00814703011436

TOTAL JOINT ORTHOPEDICS, INC.

Press-fit hip femur prosthesis, one-piece
Primary Device ID00814703011436
NIH Device Record Keyb3307234-9bf8-4e92-b64d-8baa9ee07314
Commercial Distribution StatusIn Commercial Distribution
Brand NameKlassic HD Hip System Offset Femoral Stem, Porous, size 7
Version Model Number3103.07.000
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(801)486-6070
Emailudi@tjoinc.com
Phone+1(801)486-6070
Emailudi@tjoinc.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature
Special Storage Condition, SpecifyBetween 0 and 0 *The Klassic HD Hip System should be stored in a clean, dry location at room temperature

Device Identifiers

Device Issuing AgencyDevice ID
GS100814703011436 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LWJProsthesis, hip, semi-constrained, metal/polymer, uncemented

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[00814703011436]

Radiation Sterilization


[00814703011436]

Radiation Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-21

Devices Manufactured by TOTAL JOINT ORTHOPEDICS, INC.

00810094701246 - Klassic Tibial Baseplate, Revision2025-05-15 Tibial Baseplate, Revision, Sz 1
00810094701307 - Klassic Tibial Baseplate, Revision2025-05-15 Tibial Baseplate Assembly, Revision, Sz 1 This contains the following implant numbers: 6200.01.000 Klassic Tibial Baseplate, Rev
00810094692278 - Universal Cone Impactor Head2025-05-02 Cone Impactor Head, Size 1-2, 12°
00810094692285 - Universal Cone Impactor Head2025-05-02 Cone Impactor Head, Size 3-4, 18°
00810094692292 - Universal Cone Impactor Head2025-05-02 Cone Impactor Head, Size 5-7, 24°
00810094692308 - Cone Reamer Guide2025-05-02 Cone Reamer Guide, 100mm
00810094692315 - Cone Reamer Guide2025-05-02 Cone Reamer Guide, 75mm
00810094692452 - Klassic ONE Universal Cone & Revision Baseplate Instrumentation Tray2025-05-02 Cone & Revision Baseplate Instrumentation Tray

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.