• 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 
 > 
 
16 records meeting your search criteria returned- Product Code: MCW Patient Problem: Restenosis Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARDIOVASCULAR SYSTEMS, INC. (ABBOTT) DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 01/24/2024
MEDTRONIC IRELAND SILVERHAWK BTK 01/17/2024
COVIDIEN SILVERHAWK ATK 12/20/2023
COVIDIEN SILVERHAWK BTK 12/20/2023
COVIDIEN SILVERHAWK ATK 12/20/2023
MEDTRONIC IRELAND HAWKONE 05/26/2023
MEDTRONIC IRELAND HAWKONE 12/09/2022
THE SPECTRANETICS CORPORATION SPECTRANETICS TURBO-POWER LASER ATHERECT 08/31/2022
MEDTRONIC IRELAND SILVERHAWK BTK 07/28/2022
MEDTRONIC IRELAND BTK TURBOHAWK 07/28/2022
-
-