• 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 
 7 
 8 
 9 
 10 
 > 
 
93 records meeting your search criteria returned- Product Code: KRO Patient Problem: No Clinical Signs, Symptoms or Conditions Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG ENDURO TIBIAL COMP.OFFSET CEMENTED T2 07/26/2021
AESCULAP AG ENDURO TIBIA HEMI-WEDGE T2 4MM RM/LL 07/26/2021
AESCULAP AG ENDURO TIBIA HEMI-WEDGE T2 4MM RL/LM 07/26/2021
AESCULAP AG ENDURO TIBIAL COMP.OFFSET CEMENTED T1 07/21/2021
AESCULAP AG ENDURO TIBIAL COMP.OFFSET CEMENTED T1 07/21/2021
WALDEMAR LINK GMBH & CO. KG FEMORAL COMPONENT CONDYLAR REPLACEMENT M 07/21/2021
STANMORE IMPLANTS WORLDWIDE DISTAL FEMUR JTS - TIBIAL COMPONENT 07/15/2021
AESCULAP AG AS NUT F/FEMUR EXTENS.STEM ALL SZ.NEUTR. 07/08/2021
AESCULAP AG ENDURO TIBIA HEMI-WEDGE T3 4MM RL/LM 07/01/2021
AESCULAP AG ENDURO TIBIA HEMI-WEDGE T3 4MM RM/LL 07/01/2021
-
-