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
 

 
 
 1 
 2 
 
 
11 records meeting your search criteria returned- Product Code: LKK Product Problem: Retraction Problem Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/15/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ASCENDA 01/26/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/16/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ASCENDA 09/08/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ASCENDA 04/07/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/23/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 02/19/2020
MEDTRONIC NEUROMODULATION SYNCHROMED II 10/17/2019
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 07/26/2018
MEDTRONIC NEUROMODULATION ASCENDA 07/17/2018
-
-