• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
183 records meeting your search criteria returned- Product Code: NPJ Patient Problem: Pain 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 4 02/22/2017
MAKO SURGICAL CORP. MCK FEMORAL-RM-LL-SZ 5 02/22/2017
SMITH & NEPHEW, INC. DEUCE KNEE OXINIUM FEMORAL SZ 8 12/19/2016
MAKO SURGICAL CORP. MCK TIBIAL BASEPLATE-RM/LL-SZ 5 07/26/2016
MAKO SURGICAL CORP. MCK TIBIAL BASEPLATE-LM/RL-SZ 4 07/20/2016
MAKO SURGICAL CORP. MCK FEMORAL-LM-RL-SZ 3 07/20/2016
MAKO SURGICAL CORP. MCK FEMORAL-RM-LL-SZ 2 06/26/2016
CONFORMIS, INC. IDUO 06/23/2016
MAKO SURGICAL CORP. MCK TIBIAL ONLAY INSERT-SZ 3-8MM 06/07/2016
MAKO SURGICAL CORP. MCK PATELLOFEMORAL-R-SZ 3 03/28/2016
-
-