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
 

 
 
 1 
 2 
 > 
 
12 records meeting your search criteria returned- Product Code: MAX Patient Problem: Patient Problem/Medical Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SEASPINE INC. SEASPINE SKIPJACK SYSTEM 08/27/2020
SEASPINE INC. REGATTA LATERAL SYSTEM 07/10/2020
MEDTRONIC SOFAMOR DANEK USA, INC. VERTE-STACK SPINAL SYSTEM 06/23/2020
SEASPINE INC. SEASPINE SPACER SYSTEM - HOLLYWOOD VI NA 04/13/2020
TYBER MEDICAL CONCORD PROTI 01/06/2020
MDT SOFAMOR DANEK PUERTO RICO MFG CAPSTONE SPINAL SYSTEM 11/29/2019
MEDACTA INTERNATIONAL SA MECTALIF OBLIQUE (TI PEEK) OBLIQUE INTER 05/15/2019
AESCULAP AG TSPACE PEEK IMPLANT 5° 26X11.5X9MM 05/08/2019
AESCULAP AG PROSPACE XP IMPLANT 5° 8X8.5X22MM 04/23/2019
TITAN SPINE ENDOSKELETON® TO NANOLOCK® 04/02/2019
-
-