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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
116 records meeting your search criteria returned- Product Code: MAI Product Problem: Activation, Positioning or Separation Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/12 DEGRE 10/13/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/12 DEGRE 10/12/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR, 12-DEGREE 10/12/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/12 DEGRE 10/11/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/27 DEGRE 08/30/2017
DEPUY MITEK UNKNOWN OMNISPAN NEEDLE 08/22/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR, 12-DEGREE 08/03/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/0 DEGREE 06/21/2017
ARTHREX, INC. BIO-COMP INTERFERENCE SCREW W/DISPOSABLE 01/20/2017
DEPUY MITEK OMNISPAN MENISCAL REPAIR SYSTEM/27 DEGRE 12/07/2016
-
-