• 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 20 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]
reach hip component BIOMET, INC. K982367 08/24/1998
custom flanged acetabular component BIOMET, INC. K983035 11/23/1998
apf porous coated line extension BIOMET, INC. K984154 02/11/1999
130 modified integral femoral component BIOMET, INC. K984408 02/12/1999
lateralized intergral porous primary femoral component BIOMET, INC. K984296 02/18/1999
titanium low profile screws BIOMET, INC. K991807 07/08/1999
tri-polar system BIOMET, INC. K991990 09/10/1999
modular reach hip BIOMET, INC. K994038 12/22/1999
impact modular total hip system BIOMET, INC. K000334 02/16/2000
mallory-head modular calcar total hip system BIOMET, INC. K000335 02/25/2000
-
-