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 14 Results
ProductCode: KWA Applicant: BIOMET, INC Decision Date To: 02/01/2015
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 14 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]
taperloc complete BIOMET, INC. K101086 09/03/2010
ringloc + hybrid acetabular system BIOMET, INC. K093235 04/30/2010
biomet modular femoral revision system BIOMET, INC. K090757 09/25/2009
biomet metal-on-metal hip systems- expanded contraindications BIOMET, INC. K082446 10/15/2008
porous coated acetabular components BIOMET, INC. K050124 10/04/2005
compress segmental femoral replacement system BIOMET, INC. K043547 08/05/2005
taper 2 porous femoral stem BIOMET, INC. K050441 06/29/2005
balance hip system BIOMET, INC. K050251 05/27/2005
mallory-head modular calcar stems with interlocking slots BIOMET, INC. K042774 01/21/2005
m2a/c2a acetabular system BIOMET, INC. K042841 12/21/2004
-
-