Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
1 to 10 of 50 Results
ProductCode: JWH Applicant: BIOMET, INC Decision Date To: 12/03/2016
 
 1 
 2 
 3 
 4 
 5 
 > 
Results per Page
New Search  
Export all 50 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
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
-
-