BIOMET KNEE 32-341623

GUDID 00880304536845

Biomet Orthopedics, LLC

Knee tibia prosthesis trial
Primary Device ID00880304536845
NIH Device Record Key36fbdce3-03fa-4438-9b4d-192de76f63fe
Commercial Distribution StatusIn Commercial Distribution
Brand NameBIOMET KNEE
Version Model Number32-341623
Catalog Number32-341623
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 Datefalse
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
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 Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304536845 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


[00880304536845]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-02-07
Device Publish Date2016-09-21

On-Brand Devices [BIOMET KNEE]

0088030454131332-341617
0088030453701932-148153
0088030453699932-341619
0088030453698232-148147
0088030453697532-341639
0088030453696832-148149
0088030453695132-148151
0088030453691332-341621
0088030453684532-341623
0088030453682132-341637
0088030445963232-341640
0088030445962532-341638
0088030445961832-341636
0088030445960132-341634
0088030445959532-341632
0088030445309832-148140
0088030445308132-148148
0088030445307432-148150
0088030445306732-148142
0088030445305032-148152
0088030445304332-148146
0088030445303632-148154
0088030445302932-148144
0088030432453432-341620
0088030432452732-341612
0088030432451032-341610
0088030401139732-341624
0088030401138032-341622
0088030400895332-341616
0088030400894632-341614
0088030400043832-341618

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