• 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 18 of 18 Results
ProductCode: LPH Applicant: BIOMET MANUFACTURING CORP. Decision Date To: 04/24/2024
 < 
 1 
 2 
 
Results per Page
New Search  
Export all 18 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]
parallel-sided extensively coated femoral stems BIOMET MANUFACTURING CORP. K073637 03/20/2008
biolox delta ceramic heads with 100kgy e-poly acetabular liners BIOMET MANUFACTURING CORP. K073102 11/27/2007
lateralized taperloc microplasty femoral components BIOMET MANUFACTURING CORP. K062994 03/09/2007
altra fx hip system BIOMET MANUFACTURING CORP. K063614 02/20/2007
compress segmental femoral replacement system (short spindle and anchor plug) BIOMET MANUFACTURING CORP. K062998 01/19/2007
altra press-fit hip system BIOMET MANUFACTURING CORP. K063002 10/31/2006
porous titanium acetabular shells BIOMET MANUFACTURING CORP. K052996 04/28/2006
porous titanium acetabular augments BIOMET MANUFACTURING CORP. K052888 12/06/2005
-
-