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

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
 

 
 
9 records meeting your search criteria returned- Product Code: KWQ Patient Problem: Neurological Deficit/Dysfunction Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
WARSAW ORTHOPEDICS ORION 04/21/2020
MEDOS INTERNATIONAL SàRL CH UNKNOWN PLATES 12/16/2019
MDT SOFAMOR DANEK PUERTO RICO MFG ZEPHIR ANTERIOR CERVICAL SYSTEM 01/03/2017
WARSAW ORTHOPEDICS ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM 04/09/2015
WARSAW ORTHOPEDICS ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM 11/24/2014
WARSAW ORTHOPEDICS ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM 11/23/2014
MEDTRONIC SOFAMOR DANEK ZEPHIR ANTERIOR CERVICAL PLATE SYSTEM 07/17/2014
MEDTRONIC SOFAMOR DANEK ZEPHIR ANTERIOR CERVICAL PLATE SYSTEM 07/17/2014
NUVASIVE, INC. NUVASIVE MAXCESS RETRACTOR SYSTEM 02/13/2014
-
-