• 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
-
51 to 60 of 63 Results
ProductCode: LPH Applicant: BIOMET, INC. Decision Date To: 03/28/2024
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
Results per Page
New Search  
Export all 63 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]
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 12/14 taper femoral components BIOMET, INC. K043537 01/14/2005
taperloc complete BIOMET, INC. K101086 09/03/2010
taperloc femoral stem and universal acetabular com BIOMET, INC. K921301 02/16/1994
titanium low profile screws BIOMET, INC. K991807 07/08/1999
tri-polar system BIOMET, INC. K991990 09/10/1999
-
-