VANGUARD KNEE SYSTEM 185102

GUDID 00880304441194

Biomet Orthopedics, LLC

Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis
Primary Device ID00880304441194
NIH Device Record Key87f73601-b1e7-4e0f-8dea-577ebc9a4851
Commercial Distribution StatusIn Commercial Distribution
Brand NameVANGUARD KNEE SYSTEM
Version Model Number185102
Catalog Number185102
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 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(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
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
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS100880304441194 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [VANGUARD KNEE SYSTEM]

00880304928022183401
00880304680654183523
00880304680647183521
00880304680623183501
00880304680616183483
00880304680609183481
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00880304680586183461
00880304680579183443
00880304680562183441
00880304680555183423
00880304680548183421
00880304680531183403
00880304674851189123
00880304674844189121
00880304674837189103
00880304674820189101
00880304674813189083
00880304674806189081
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00880304674783189061
00880304674776189043
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00880304674752189023
00880304674745189021
00880304674738189003
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00880304673854183563
00880304673847183561
00880304673830183543
00880304673823183541
00880304653849CP113649
00880304653832CP113648
00880304653825CP113647
00880304653818CP113646
00880304653801CP113645
00880304653795CP113644
00880304653788CP113643

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