• 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 42 Results
ProductCode: JWH Applicant: BIOMET, INC Decision Date To: 10/23/2014
 
 1 
 2 
 3 
 4 
 5 
 > 
Results per Page
New Search
Export all 42 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 360 osseoti tibial sleeve augme biomet, inc. K140883 07/30/2014
e1 series a patellae, standard 3-peg, e1 biomet, inc. K140902 07/03/2014
vanguard xp knee system biomet, inc. K132873 12/11/2013
patient-specific vanguard femoral compon biomet, inc. K102125 02/23/2011
vanguard 360 revision knee system biomet, inc. K093293 10/22/2010
regenerex tibial components biomet, inc. K080361 04/21/2008
vanguard knee system titanium femoral co biomet, inc. K080204 03/20/2008
vanguard anterior stabilized tibial bear biomet, inc. K050222 08/16/2005
disposable cement spacer molds for tempo biomet, inc. K050210 07/19/2005
vanguard ssk knee system biomet, inc. K042757 02/11/2005
-
-