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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
133 records meeting your search criteria returned- Product Code: NKB Product Problem: Mechanical Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SEASPINE INC. MARINER PEDICLE SCREW SYSTEM 06/22/2020
SEASPINE INC. MARINER 03/16/2020
SEASPINE INC. MARINER 03/16/2020
SEASPINE INC. MARINER 03/16/2020
SEASPINE INC. MARINER 03/16/2020
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SPINAL SYSTEM 03/05/2020
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SPINAL SYSTEM 03/05/2020
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SPINAL SYSTEM 03/05/2020
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 03/05/2020
WARSAW ORTHOPEDICS CD HORIZON SPINAL SYSTEM 03/05/2020
-
-