Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 16 Results
ProductCode: MBL Applicant: SMITH & NEPHEW, INC. Decision Date To: 05/21/2024
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 16 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]
smith & nephew hip systems Smith & Nephew, Inc. K211176 07/01/2022
r3 ha coated acetabular shells Smith & Nephew, Inc. K201701 10/06/2020
r3 anteverted liners Smith & Nephew, Inc. K182535 11/19/2018
redapt modular acetabular shell Smith & Nephew, Inc. K182109 11/16/2018
oxinium dh fermoral heads SMITH & NEPHEW, INC. K161233 12/14/2016
smith & nephew global femoral head trials SMITH & NEPHEW, INC. K132435 10/22/2013
smith & nephew, inc. hip system instrumentation SMITH & NEPHEW, INC. K123598 06/28/2013
r3 xlpe liners SMITH & NEPHEW, INC. K113848 04/27/2012
r3 xlpe anteverted liners SMITH & NEPHEW, INC. K102370 01/19/2011
slr-plus standard and lateral femoral stems SMITH & NEPHEW, INC. K093991 04/15/2010
-
-