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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
114 records meeting your search criteria returned- Product Code: NPJ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAKO SURGICAL CORP. MCK TIBIAL BASEPLATE-RM/LL-SZ 1 06/02/2017
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 3-8MM 05/22/2017
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 3-9MM 05/22/2017
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 6-8MM 04/10/2017
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 5-8MM 03/28/2017
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 3-9MM 03/28/2017
STRYKER ORTHOPAEDICS-MAHWAH MCK TIBIAL ONLAY INSERT-SZ 3-10MM 03/27/2017
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN TIBIAL ONLAY 03/27/2017
CONFORMIS, INC. IDUO G2 02/21/2017
CONFORMIS, INC. IDUO G2 02/07/2017
-
-