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 
 > 
 
18 records meeting your search criteria returned- Product Code: PHX Patient Problem: Pulmonary Embolism Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 UNK SHOULDER HUMERAL CUP DELTA XTEND 09/17/2021
DEPUY IRELAND - 9616671 UNK SHOULDER HUMERAL STEM DELTA XTEND 09/17/2021
DEPUY IRELAND - 9616671 UNK SHOULDER GLENOSPHERE DELTA XTEND 09/17/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN SHOULDER METAGLENE 09/17/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN SHOULDER LOCKING SCREW 09/17/2021
DEPUY IRELAND - 9616671 UNK SHOULDER HUMERAL EPIPHYSIS DELTA XTE 09/17/2021
DEPUY ORTHOPAEDICS INC US UNKNOWN SHOULDER LOCKING SCREW 09/17/2021
ARTHREX, INC. 36 +3 / 33 COMBO HUMERAL INSERT 03/15/2021
ARTHREX, INC. 33 +4 LAT/24 GLENOSPHERE 03/15/2021
ARTHREX, INC. 24MM BASEPLATE, 10 FULL AUGMENT 03/15/2021
-
-