• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
147 records meeting your search criteria returned- Product Code: MNI Product Problem: Fracture Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG S4 SET SCREW NEW VERSION 09/18/2020
AESCULAP AG S4 SET SCREW NEW VERSION 09/16/2020
MEDICREA INTERNATIONAL PASS LP 10/07/2019
Unknown Manufacturer SPINCAL FUSION RELATED HARDWARE 09/17/2019
AESCULAP AG SSE 5.2 TI ROD 70MM 08/02/2019
X-SPINE SYSTEMS, INC. XPRESS MINIMALLY INVASIVE PEDICLE SCREW 07/25/2019
MEDICREA INTERNATIONAL PASS LP 07/15/2019
MEDICREA INTERNATIONAL PASS LP 07/03/2019
X-SPINE SYSTEMS, INC. XPRESS MINIAMALLY INVASIVE PEDICLE SCREW 07/02/2019
K2M INC. EVEREST SPINAL SYSTEM 06/03/2019
-
-