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

Premarket Approval (PMA)
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameANGIOLINK VASCULAR CLOSURE SYSTEM
Classification Namedevice, hemostasis, vascular
Generic Namevascular hemostasis device
ApplicantMEDTRONIC VASCULAR
PMA NumberP040022
Supplement NumberS003
Date Received03/19/2007
Decision Date05/24/2007
Product Code
MGB[ Registered Establishments with MGB ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for incorporation of the following processing and material changes to the distal end of the vcs 1000 dilator: 1) change in the dilator material from nylon 11 to pebax nylon 4033 for the dilator distal tip and from nylon 11 to pebax nylon 6033 for the dilator distal shaft; 2) addition of a rf and/or alternative thermal energy source to bond the dilator distal tip to the distal shaft; and 3) addition of a heat shrink sleeve to enhance the bond between the shaft and the distal tip.
-
-