• 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 
 > 
 
32 records meeting your search criteria returned- Product Code: NKB Patient Problem: Unspecified Nervous System Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDOS INTERNATIONAL SàRL CH UNK - SCREWS: SKYLINE 02/10/2023
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 11/14/2022
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 11/14/2022
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 11/14/2022
MEDTRONIC SOFAMOR DANEK USA, INC CD HORIZON SPINAL SYSTEM 10/27/2022
MEDOS INTERNATIONAL SàRL CH UNK - CONSTRUCTS: EXPEDIUM VERSE 10/17/2022
SYNTHES GMBH UNK - CONSTRUCTS: MATRIX 10/17/2022
MDT SOFAMOR DANEK PUERTO RICO MFG CD HORIZON SOLERA VOYAGER SPINAL SYSTEM 04/01/2021
MEDOS INTERNATIONAL SàRL CH SINGLE-INNER SETSCREW 05/12/2020
MEDOS INTERNATIONAL SàRL CH SINGLE-INNER SETSCREW 05/12/2020
-
-