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 5 of 5 Results
510(K) Number: K082650
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 Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended... 2 08/24/2015 Synthes (USA) Products LLC
Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components. 2 06/19/2014 Synthes, Inc.
Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007, Lot Number... 2 07/29/2013 Synthes USA HQ, Inc.
Large Combination Clamp/Large External Fixation System, Part Number 390.005 Product Usage: Synth... 2 03/11/2013 Synthes USA HQ, Inc.
Synthes External Fixation System Tube to Tube Clamp, Part Number 390.007. Intended for use to pro... 2 11/13/2012 Synthes USA HQ, Inc.
-
-