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

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 
 
 
38 records meeting your search criteria returned- Product Code: KKY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION HTR-PATIENT MATCHED RIGHT FRONTAL SPHENO 09/29/2016
BIOMET MICROFIXATION HTR-PATIENT MATCH IMPLANT WELCH LEFT FRO 06/01/2016
STRYKER ORTHOPAEDICS-MAHWAH CMF CUSTOMIZED IMPLANT KIT LARGE 02/24/2016
STRYKER ORTHOPAEDICS-MAHWAH CMF CUSTOMIZED IMPLANT KIT LARGE 02/24/2016
BIOMET MICROFIXATION HTR-PMI LEFT FRONTAL SPHENOID PARIETAL T 01/14/2016
BIOMET MICROFIXATION HTR-PMI RIGHT FRONTAL SPHENOID PARIETAL 12/16/2015
BIOMET MICROFIXATION HTR-PMI RIGHT FRONT SP PAR TE 12/15/2015
BIOMET MICROFIXATION HARD TISSUE REPLACE(HTR(R))-PATIENT-MATC 04/16/2015
-
-