• 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 27 Results
ProductCode: MEH Applicant: SMITH & NEPHEW, INC Decision Date To: 09/19/2019
 
 1 
 2 
 3 
 > 
Results per Page
New Search  
Export all 27 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]
redapt¿ revision femoral system SMITH & NEPHEW, INC. K151902 09/03/2015
polarstem collared (standard and lateral) and valgus femoral stem with ti/ha SMITH & NEPHEW, INC. K143739 04/20/2015
smith & nephew global femoral head trials SMITH & NEPHEW, INC. K132435 10/22/2013
polarstem standard and lateral femoral stems with ti/ha SMITH & NEPHEW, INC. K130728 10/10/2013
smith & nephew, inc. hip system instrumentation SMITH & NEPHEW, INC. K123598 06/28/2013
smith & nephew redapt revision femoral system SMITH & NEPHEW, INC. K121627 10/15/2012
smith & nephew radiopaque trial necks SMITH & NEPHEW, INC. K113039 10/05/2012
r3 xlpe liners SMITH & NEPHEW, INC. K113848 04/27/2012
modular proximally fluted hip stem SMITH & NEPHEW, INC. K113789 04/19/2012
smith & nephew mdf modular sleeve SMITH & NEPHEW, INC. K100481 07/15/2010
-
-