• 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 
 > 
 
21 records meeting your search criteria returned- Product Code: MJO Patient Problem: Inadequate Pain Relief Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SPINAL KINETICS M6-C 03/25/2023
SPINAL KINETICS M6-C 03/25/2023
SPINAL KINETICS M6-C 03/25/2023
CENTINEL SPINE PRODISC C US IMPLANT MEDIUM 5MM 03/20/2023
CENTINEL SPINE PRODISC C US IMPLANT MEDIUM 5MM 03/20/2023
CENTINEL SPINE PRODISC L PE INLAY M 10 03/08/2023
CENTINEL SPINE PRODISC L INFERIOR END PLATE MED 0 03/08/2023
SYNTHES BRANDYWINE PRODISC L SUPERIOR END PLATE MED 11 03/08/2023
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD 15X15 H5 US 02/24/2023
SPINAL KINETICS M6-C 02/23/2023
-
-