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 8 of 8 Results
ProductCode: MBV Applicant: BIOMET, INC. Decision Date To: 05/10/2024
Results per Page
New Search  
Export all 8 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. K153657 05/10/2016
vanguard 360 revision knee system Biomet, Inc. K143192 02/12/2015
biomet tibial trays BIOMET, INC. K142933 12/23/2014
vanguard xp femoral component(gen ii)/vanguard xp femoral trial BIOMET, INC. K141407 10/27/2014
e1 series a patellae, standard 3-peg, e1 series a patellae, thin 3-peg, e1 series patellae, asymmetrical, 3-peg BIOMET, INC. K140902 07/03/2014
vanguard xp knee system BIOMET, INC. K132873 12/11/2013
vanguard 360 revision knee system BIOMET, INC. K093293 10/22/2010
offset tibial tray BIOMET, INC. K010212 02/14/2001
-
-