VANGUARD SSK360/DA360 KNEE SYSTEM 185264

GUDID 00880304481954

Biomet Orthopedics, LLC

Uncoated knee femur prosthesis, metallic
Primary Device ID00880304481954
NIH Device Record Keyb3794236-0fd3-433e-8d43-bf3e744a2274
Commercial Distribution StatusIn Commercial Distribution
Brand NameVANGUARD SSK360/DA360 KNEE SYSTEM
Version Model Number185264
Catalog Number185264
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100880304481954 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBVProsthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-12-11
Device Publish Date2015-10-24

On-Brand Devices [VANGUARD SSK360/DA360 KNEE SYSTEM]

00880304482128185287
00880304482111185285
00880304482104185283
00880304482098185281
00880304482081185290
00880304482074185288
00880304482067185286
00880304482050185284
00880304482043185282
00880304482036185280
00880304482029185267
00880304482012185265
00880304482005185263
00880304481992185261
00880304481985185270
00880304481978185268
00880304481961185266
00880304481954185264
00880304481947185262
00880304467422185260

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