• 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 38 of 38 Results
ProductCode: LPH Applicant: HOWMEDICA OSTEONICS CORP Decision Date To: 11/28/2022
 < 
 1 
 2 
 3 
 4 
 
Results per Page
New Search  
Export all 38 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]
stryker modular hip system HOWMEDICA OSTEONICS CORP K071082 09/13/2007
system 12 x3 acetabular inserts; series ii x3 acetabular inserts HOWMEDICA OSTEONICS CORP K052748 12/02/2005
trident acetabular system HOWMEDICA OSTEONICS CORP K033716 02/10/2005
trident large diameter acetabular inserts HOWMEDICA OSTEONICS CORP K062419 11/15/2006
trident large diameter hip system HOWMEDICA OSTEONICS CORP K061434 08/22/2006
tritanium non-modular shell & x3 all-poly insert HOWMEDICA OSTEONICS CORP K090897 10/23/2009
tritanium acetabular shell system HOWMEDICA OSTEONICS CORP K081171 07/22/2008
tritanium peri-apatitie acetabular solid-backed shell, tritanium peri-apatite HOWMEDICA OSTEONICS CORP K101072 04/11/2011
-
-