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 21 Results
ProductCode: KWY Applicant: BIOMET, INC. Decision Date To: 06/08/2024
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 21 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]
stageone™ select hip cement spacer molds Biomet, Inc. K222760 12/28/2022
stageone select cement spacer molds for temporary hip replacement BIOMET, INC. K161166 09/08/2016
arcos one-piece femoral revision system Biomet, Inc. K151603 10/06/2015
g7 dual mobility system BIOMET, INC. K150522 05/01/2015
echo bi-metric microplasty line extension BIOMET, INC. K150503 03/25/2015
echo bi-metric microplasty hip system BIOMET, INC. K143009 12/18/2014
sirius femoral stem, size 30a Biomet, Inc. K142295 09/15/2014
sirius femoral stem BIOMET, INC. K130610 08/30/2013
arcos trochanter button BIOMET, INC. K130063 04/19/2013
taperloc complete BIOMET, INC. K101086 09/03/2010
-
-