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

510(K) Premarket Notification
  • Print
  • Share
  • E-mail
-
321 to 330 of 500 Results *
 < 
 32 
 33 
 34 
 35 
 36 
 37 
 38 
 39 
 40 
 41 
 > 
results per page
New Searchexport reports to excelExport to Excel | HelpHelp
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by PMA Number [0-9]
Sort by PMA Number [9-0]
510(K)
Number
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
headstar medical small volume jet nebulizer HEADSTAR MEDICAL PRODUCTS CO., LTD k121770 04/17/2013
stingray cervical cage OMNI SURGICAL, LP DBA SPINE360 k122085 10/17/2012
ufit ten-10 BIOSIGN TECHNOLOGIES, INC. k122443 11/20/2012
sentrysuite product line CAREFUSION GERMANY 234 GMBH k122699 11/19/2012
hammer toe implant TRILLIANT SURGICAL LTD k122959 11/07/2012
arthrex fracture plates ARTHREX, INC. k123241 04/05/2013
juggerknotless soft anchors, juggerknotless m soft anchors, juggerknotless soft anchors with needles, juggerknotless sof BIOMET SPORTS MEDICINE k123485 03/18/2013
shuntcheck NEURODX DEVELOPMENT LLC k123554 03/07/2013
acleara, theraclear THERAVANT CORPORATION k123889 03/04/2013
sta compact max DIAGNOSTICA STAGO, INCORPORATED k130090 02/12/2013

*   The maximum 500 records meeting your search criteria returned. Please narrow your search.
-
-