• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
54 records meeting your search criteria returned- Product Code: KRO Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ARTICULAR SURFACE WITH HINGE POST EXTENS 02/24/2020
AESCULAP AG ENDURO FEMORAL COMPONENT CEMENTED F2L 07/11/2019
AESCULAP AG AS ENDURO FEM.SPACER POST/DIST F2 4X8MM 04/10/2019
AESCULAP AG AS NUT F/FEMUR EXTENS.STEM ALL SZ.NEUTR. 04/10/2019
AESCULAP AG AS ENDURO FEM.SPACER POST/DIST F2 4X8MM 04/10/2019
AESCULAP AG AS TIBIA OFFSET STEM D12X92MM CEMENTED 04/10/2019
AESCULAP AG AS FEMUR EXTENS.STEM 6° D18X77 CEMENTED 04/10/2019
AESCULAP AG AS ENDURO TIBIA HEMI-WEDGE T1 4MM RM/LL 04/10/2019
AESCULAP AG AS ENDURO TIBIA HEMI-WEDGE T1 4MM RL/LM 04/10/2019
AESCULAP AG AS ENDURO FEMORAL COMPONENT CEMENTED F2L 04/10/2019
-
-