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
 

 
 
8 records meeting your search criteria returned- Product Code: PHM Report Date From: 1/1/2022 Report Date To: 12/31/2022
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NUVASIVE, INC. NUVASIVE COROENT THORACOLUMBAR INTERBODY 11/18/2022
NUVASIVE, INC. NUVASIVE COROENT THORACOLUMBAR INTERBODY 10/29/2022
NUVASIVE, INC. NUVASIVE COROENT THORACOLUMBAR INTERBODY 10/10/2022
NUVASIVE, INC. NUVASIVE COROENT THORACOLUMBAR INTERBODY 10/10/2022
NUVASIVE, INCORPORATED NUVASIVE COROENT THORACOLUMBAR IMPLANTS 09/20/2022
NUVASIVE, INCORPORATED NUVASIVE COROENT THORACOLUMBAR IMPLANTS 07/12/2022
NUVASIVE, INCORPORATED NUVASIVE COROENT THORACOLUMBAR IMPLANTS 06/02/2022
NUVASIVE, INC. NUVASIVE COROENT THORACOLUMBAR INTERBODY 02/11/2022
-
-