PMA P040037S130

Device
GORE VIABAHN Endoprosthesis and GORE VIABAHN Endoprosthesis with Heparin Bioactive Surface
Applicant
W. L. Gore & Associates, Inc.
Product code
NIP
Decision date
2019-10-02
Generic name
STENT, SUPERFICIAL FEMORAL ARTERY
Approval order statement
Approval to implement changes to your divisional bacterial endotoxin test parameters using the Limulus Amebocyte Lysate test methodology.

Current openFDA PMA Record#

Device
GORE VIABAHN Endoprosthesis and GORE VIABAHN Endoprosthesis with Heparin Bioactive Surface
Applicant
W. L. Gore & Associates, Inc.
PMA number
P040037
Supplement
S130
Product code
NIP
Generic name
STENT, SUPERFICIAL FEMORAL ARTERY
Decision date
2019-10-02
Decision code
APPR
Date received
2019-03-12
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Approval to implement changes to your divisional bacterial endotoxin test parameters using the Limulus Amebocyte Lysate test methodology.