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

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
1 to 3 of 3 Results
510(K) Number: K110789
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
Synthes Application Instrument for Sternal ZIPFIX. Indications for use include primary or secondar... 2 11/14/2015 FEI # 3008812560
Synthes (USA) Products LLC
Synthes Application Instrument for Sternal ZIPFIX; indications for use include primary or secondary ... 2 08/27/2015 FEI # 3008812560
Synthes (USA) Products LLC
Synthes Application Instrument Sternal Zip Flex System intended for use in primary or secondary c... 2 10/30/2013 FEI # 3005180112
Synthes USA HQ, Inc.
-
-