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
 

 
 < 
 1 
 2 
 3 
 
 
29 records meeting your search criteria returned- Product Code: PBI Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET ORTHOPEDICS G7 ACETABULAR SCREW 6.5MM X 30MM 09/14/2016
BIOMET ORTHOPEDICS G7 ACETABULAR SHELL 3 HOLE POROUS PLASMA 09/14/2016
BIOMET ORTHOPEDICS G7 PPS LTD ACET SHELL 50D 07/26/2016
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 20MM 07/09/2016
BIOMET ORTHOPEDICS G7 SCREW 6.5MM X 20MM 07/09/2016
BIOMET ORTHOPEDICS G7 HI-WALL E1 LINER 32MM E 06/03/2016
BIOMET ORTHOPEDICS G7 PPS LTD ACET SHELL 54F 06/02/2016
BIOMET ORTHOPEDICS G7 PPS LTD ACET SHELL 50D 05/27/2016
BIOMET UK LTD G7 HI-WALL E1 LINER 40MM F 11/25/2015
-
-