PMA P980033S010

Device
WALLSTENT (TIPS AND VENOUS) ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
Applicant
Boston Scientific Corporation
PMA number
P980033
Supplement
S010
Product code
QKJ
Decision date
2004-05-07
Classification
Stent, Coronary
Generic name
Stent, central venous
Approval order statement
CHANGE IN THE MANUFACTURING MATERIAL USED IN THE MANUFACTURE OF THE EXTERIOR TUBE FOR THE DEVICE.

Current openFDA PMA Record#

Device
WALLSTENT (TIPS AND VENOUS) ENDOPROSTHESIS WITH UNISTEP PLUS DELIVERY SYSTEM
Applicant
Boston Scientific Corporation
PMA number
P980033
Supplement
S010
Product code
QKJ
Generic name
Stent, central venous
Decision date
2004-05-07
Decision code
OK30
Date received
2004-04-09
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
CHANGE IN THE MANUFACTURING MATERIAL USED IN THE MANUFACTURE OF THE EXTERIOR TUBE FOR THE DEVICE.