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 NamePROSTAR TM 8FR AND 10FR PVS AND PROSTAR XL
ApplicantABBOTT VASCULAR INC.
PMA NumberP960043
Supplement NumberS002
Date Received06/02/1997
Decision Date12/29/1997
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for modified percutaneous vascular surgical (pvs) systems. The devices, as modified, will be marketed under the trade names prostar(r) plus 8 french, prostar(r) plus 10 french, and prostar(r) xl 8 french pvs systems. The prostar(r) plus and prostar(r) xl pvs systems consist of a pvs device and a perclose(r) knot pusher. The prostar(r) plus and prostart(r) xl pvs systems are indicated for the percutaneous deliveyr of sutures for closing the common femoral artery access site and reducing hte time to hemostasis and ambulation (patient walks ten feet) of patients who have undegone catheterization procedures using 6. 5 french to 10 french sheaths.
-
-