• 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
-
11 to 20 of 50 Results
ProductCode: JWH Applicant: BIOMET, INC Decision Date To: 10/23/2014
 < 
 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
patient-specific vanguard femoral componets 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 components BIOMET, INC. K080204 03/20/2008
vanguard anterior stabilized tibial bearings BIOMET, INC. K050222 08/16/2005
disposable cement spacer molds for temporary knee prostheses BIOMET, INC. K050210 07/19/2005
vanguard ssk knee system BIOMET, INC. K042757 02/11/2005
maxim accel (vanguard) ps+ bearings BIOMET, INC. K041046 05/21/2004
im total femur BIOMET, INC. K033871 04/16/2004
-
-