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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
146 records meeting your search criteria returned- Product Code: MEH Patient Problem: Toxicity Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER (ORTHOPAEDICS CORK LRG TAP PRI MOD NCK 8DEG 42MM 02/05/2014
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 02/03/2014
STRYKER ORTHOPAEDICS CORK LRG TAP PRI MOD NCK 0DEG 38MM 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJUVENATE MODULAR HIP IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJUVENATE MODULAR IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJVENATE MODULAR IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJUVENATE MODULAR IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJUVENATE MODULAR IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJUVENATE MODULAR IMPLANT 01/31/2014
STRYKER ORTHOPAEDICS STRYKER REJVUENATE MODULAR IMPLANT 01/31/2014
-
-