• 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
 

 
 
 1 
 2 
 3 
 4 
 5 
 > 
 
42 records meeting your search criteria returned- Product Code: NQO Report Date From: 1/1/2014 Report Date To: 12/31/2014

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC SOFAMOR DANEK USA, INC X-STOP PEEK INTERSPINOUS SPACER 12/29/2014
MEDTRONIC SOFAMOR DANEK USA, INC X-STOP PEEK INTERSPINOUS SPACER 12/29/2014
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHNOLOGY 12/19/2014
MEDTRONIC SOFAMOR DANEK USA, INC UNKNOWN MEDTRONIC ROD 12/16/2014
MEDTRONIC SOFAMOR DANEK USA, INC UNKNOWN MEDTRONIC SPACER 12/16/2014
PARADIGM SPINE GMBH COFLEX (R) INTERLAMINAR TECHNOLOGY 12/10/2014
PARADIGM SPINE GMBH COFLEX INTERLAMINAR TECHOLOGY 11/26/2014
MDT KYPHON SUNNYVALE MFG X-STOP PEEK INTERSPINOUS SPACER 11/13/2014
PARADIGM SPINE COFLEX INTERLAMINAR 10/24/2014
MEDTRONIC SOFAMOR DANEK X-STOP PEEK INTERSPINOUS SPACER 10/24/2014
-
-