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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 50 Results
ProductCode: JWH Applicant: Biomet, Inc Decision Date To: 12/05/2022
 
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510(K)
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vanguard xp knee system BIOMET, INC. K132873 12/11/2013
vanguard xp knee system BIOMET, INC. K153657 05/10/2016
vanguard xp femoral component(gen ii)/vanguard xp femoral trial BIOMET, INC. K141407 10/27/2014
vanguard ssk knee system BIOMET, INC. K042757 02/11/2005
vanguard knee system titanium femoral components BIOMET, INC. K080204 03/20/2008
vanguard anterior stabilized tibial bearings BIOMET, INC. K050222 08/16/2005
vanguard 360 revision knee system BIOMET, INC. K093293 10/22/2010
vanguard 360 revision knee system Biomet, Inc. K143192 02/12/2015
vanguard 360 osseoti tibial sleeve augment BIOMET, INC. K140883 07/30/2014
ultra high molecular weight polyethylene component BIOMET, INC. K921182 07/23/1993
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