OSS MODULAR TIBIAL TRAY TRIAL 110018672

GUDID 00880304678576

Biomet Orthopedics, LLC

Knee tibia prosthesis trial Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable Knee tibia prosthesis trial, reusable
Primary Device ID00880304678576
NIH Device Record Keyd609fff3-ed5b-4113-802f-c7c5a1ec4ba8
Commercial Distribution StatusIn Commercial Distribution
Brand NameOSS MODULAR TIBIAL TRAY TRIAL
Version Model Number110018672
Catalog Number110018672
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

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
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304678576 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


[00880304678576]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-02-07
Device Publish Date2016-10-27

On-Brand Devices [OSS MODULAR TIBIAL TRAY TRIAL]

00880304678590110018674
00880304678583110018673
00880304678576110018672
00880304678569110018671
00880304678552110018670
00880304678545110018669

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