Vanguard Removable Molded Poly Tibia SSI002122

GUDID 00880304989153

Biomet Orthopedics, LLC

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Primary Device ID00880304989153
NIH Device Record Keyd62925df-6824-4f51-8cb6-abe113eb8e08
Commercial Distribution StatusIn Commercial Distribution
Brand NameVanguard Removable Molded Poly Tibia
Version Model NumberSSI002122
Catalog NumberSSI002122
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 Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone1(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
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
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Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304989153 [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

[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


[00880304989153]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-02-07
Device Publish Date2017-05-03

On-Brand Devices [Vanguard Removable Molded Poly Tibia]

00880304989153SSI002122
00880304989146SSI002121
00880304989139SSI002120

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