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 
 > 
 
52 records meeting your search criteria returned- Product Code: LWJ Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW ORTHOPAEDICS AG POLARSTEM STEM STD TI/HA 3 NON-CEM 01/18/2023
SMITH & NEPHEW ORTHOPAEDICS AG METAL METAL BALL HEAD 22L CONE 12/14 07/22/2022
SMITH & NEPHEW ORTHOPAEDICS AG POLARSTEM COLLAR LAT. TI/HA 1 06/10/2022
DEPUY ORTHOPAEDICS INC US SUMMIT BASIC PRESS FIT SZ 5 05/31/2022
DEPUY ORTHOPAEDICS INC US SUMMIT BASIC PRESS FIT SZ 6 04/26/2022
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 04/20/2022
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 04/13/2022
DEPUY ORTHOPAEDICS INC US SUMMIT BASIC PRESS FIT SZ 4 12/20/2021
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 10/04/2021
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,18X13X160 09/29/2021
-
-