• 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 6 of 6 Results
ProductCode: MBH Applicant: BIOMET MANUFACTURING CORP Decision Date To: 03/07/2021
Results per Page
New Search  
Export all 6 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 MANUFACTURING CORP. K122160 03/20/2013
vanguard complete knee system BIOMET MANUFACTURING CORP. K113550 02/29/2012
regenerex patella components BIOMET MANUFACTURING CORP. K083782 04/03/2009
regenerex porous titanium sleeve augments BIOMET MANUFACTURING CORP. K072336 11/05/2007
vanguard ps open box porous femoral components BIOMET MANUFACTURING CORP. K060303 03/30/2006
ascent porous open box ps component/ascent posterior stabalized (ps) distal femoral pegs BIOMET MANUFACTURING CORP. K041872 09/08/2004
-
-