• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: PNW Patient Problem: Ambulation Difficulties Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARTIVA, INC CARTIVA IMPLANT 10MM 01/26/2024
CARTIVA, INC CARTIVA IMPLANT 10MM 12/19/2023
CARTIVA, INC UNKNOWN CARTIVA IMPLANT 11/07/2023
CARTIVA, INC UNKNOWN CARTIVA IMPLANT 09/01/2023
CARTIVA, INC UNKNOWN CARTIVA IMPLANT 03/24/2023
CARTIVA, INC CARTIVA SYNTHETIC CARTILAGE IMPLANT 08/16/2022
CARTIVA CARTIVA 02/25/2022
CARTIVA, INC CARTIVA SYNTHETIC CARTILAGE IMPLANT 10/27/2021
CARTIVA, INC./WRIGHT MEDICAL TECHNOLOGY, CARTIVA SYNTHETIC CARTILAGE IMPLANT 12/15/2020
WRIGHT MEDICAL / CARTIVA, INC. CARTIVIA IMPLANT 03/10/2020
-
-