• 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
-
21 to 30 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]
tritanium acetabular shell system HOWMEDICA OSTEONICS CORP K081171 07/22/2008
stryker modular hip system HOWMEDICA OSTEONICS CORP K071082 09/13/2007
pca 36mm femoral heads HOWMEDICA OSTEONICS CORP K061168 07/18/2006
trident large diameter acetabular inserts HOWMEDICA OSTEONICS CORP K062419 11/15/2006
trident large diameter hip system HOWMEDICA OSTEONICS CORP K061434 08/22/2006
modification to: restoration modular system HOWMEDICA OSTEONICS CORP. K050138 03/21/2005
restoration modular system HOWMEDICA OSTEONICS CORP K051363 06/23/2005
system 12 x3 acetabular inserts; series ii x3 acetabular inserts HOWMEDICA OSTEONICS CORP K052748 12/02/2005
modification to restoration modular system HOWMEDICA OSTEONICS CORP. K040734 08/25/2004
global modular replacement system anteverted promimal femoral component HOWMEDICA OSTEONICS CORP. K032581 10/09/2003
-
-