• 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
31 to 40 of 47 Results
ProductCode: LZO Applicant: BIOMET, INC. Decision Date To: 12/01/2022
Results per Page
New Search  
Export all 47 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]
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
reach femoral hip component BIOMET, INC. K971824 12/04/1997
reach hip component BIOMET, INC. K982367 08/24/1998
regenerx ringloc + modular acetabular shells BIOMET, INC. K070369 03/09/2007
ringloc + hybrid acetabular system BIOMET, INC. K093235 04/30/2010
ringloc bi-polar acetabular component BIOMET, INC. K051569 09/29/2005
rx90 low profile acetabular system BIOMET, INC. K042989 04/28/2005
sirius femoral stem BIOMET, INC. K130610 08/30/2013
sirius femoral stem, size 30a Biomet, Inc. K142295 09/15/2014
taper 2 porous femoral stem BIOMET, INC. K050441 06/29/2005
taperloc complete BIOMET, INC. K101086 09/03/2010