• 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 
 4 
 5 
 > 
 
50 records meeting your search criteria returned- Product Code: NKB Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG ENNOVATE OPEN LAT.OFFSET CONNECTOR 20MM 02/27/2024
MEDACTA INTERNATIONAL SA PEDICLE SCREW 03.50.054 PEDICLE SCREW 8X 06/16/2023
MEDTRONIC SOFAMOR DANEK USA, INC CD HORIZON® BALLAST¿ SPINAL SYSTEM 05/15/2023
NUVASIVE, INC. NUVASIVE RELINE SYSTEM 04/13/2023
NUVASIVE, INC. NUVASIVE RELINE SYSTEM 04/13/2023
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA SPINAL SYSTEM 02/21/2023
ZIMMER BIOMET SPINE INC. TOP LOADING POLY SCREW ASSEMBLIES 7.5X50 02/13/2023
ZIMMER BIOMET SPINE INC. TOP LOADING POLY SCREW ASSEMBLIES 6.5X50 02/13/2023
ZIMMER BIOMET SPINE INC. TOP LOADING POLY SCREW ASSEMBLIES 6.5X50 02/13/2023
MEDACTA INTERNATIONAL SA MUST LT 03.57.035 MUST LT 15MM SHORT - P 11/18/2022
-
-