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

Manufacturer and User Facility Device Experience (MAUDE)
  • 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
123 records meeting your search criteria returned- Product Code: NKB Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GLOBUS MEDICAL, INC. CREO 10/03/2022
GLOBUS MEDICAL, INC. CREO FENESTRATED SCREW SYSTEM 09/13/2022
NUVASIVE, INCORPORATED GSB GLOBAL SPINAL BALANCE SYSTEM 07/29/2022
NUVASIVE, INCORPORATED NUVASIVE RELINE SYSTEM 06/09/2022
STRYKER SPINE-US 9.5X100 POLYAXIAL SCREW 05/23/2022
K2M, INC. MESA 2 DEFORMITY POLYAXIAL SCREW; SIZE Ø 05/09/2022
K2M, INC. DEFORMITY, UNIPLANAR SCREW; SIZE Ø6.5X45 05/05/2022
INTEGRITY IMPLANTS INC, PALM BEACH GARDE LINESIDER NON-MOD STANDARD TULIP, DUAL L 04/11/2022
MEDICREA INTERNATIONAL SA UNKNOWN 04/01/2022
STRYKER SPINE-US MANTIS REDUX BLOCKER 02/18/2022
-
-