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

Manufacturer and User Facility Device Experience (MAUDE)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
68 records meeting your search criteria returned- Product Code: NXT Patient Problem: Limited Mobility Of The Implanted Joint Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 54MM 05/16/2018
SMITH & NEPHEW ORTHOPAEDICS LTD ACETLR CUP HAP 52MM W/ IMPTR 03/20/2018
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 03/20/2018
SMITH & NEPHEW ORTHOPAEDICS LTD ACETLR CUP HAP 56MM W/ IMPTR 03/16/2018
SMITH & NEPHEW ORTHOPAEDICS LTD ACETLR CUP HAP 50MM W/ IMPTR 02/12/2018
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 11/30/2017
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 50MM 10/09/2017
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 09/27/2017
SMITH & NEPHEW ORTHOPAEDICS LTD ACETLR CUP HAP 58MM W/ IMPTR 06/07/2017
SMITH & NEPHEW ORTHOPAEDICS LTD BHR ACETABULAR CUP 58MM 07/19/2016
-
-