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
 

 
 
7 records meeting your search criteria returned- Product Code: PEK Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
X-SPINE SYSTEMS, INC. AXLE INTERSPINOUS FUSION SYSTEM 05/28/2020
X-SPINE SYSTEMS, INC. AXLE INTERSPINOUS FUSION SYSTEM 04/10/2020
LDR MÉDICAL IMPLANT HOLDER 05/03/2019
X-SPINE SYSTEMS, INC. AXLE INTERSPINOUS FUSION SYSTEM 09/14/2018
X-SPINE SYSTEMS, INC. AXLE INTERSPINOUS FUSION SYSTEM 09/04/2018
STRYKER SPINE-SWITZERLAND UNIVISE SPINOUS PROCESS FIXATION PLATE, 01/13/2014
STRYKER SPINE-SWITZERLAND UNIVISE SPINOUS PROCESS FIXATION PLATE, 01/08/2014
-
-