PMA P220021S006

Device
DETOUR System
Applicant
Endologix, LLC
PMA number
P220021
Supplement
S006
Product code
QWM
Decision date
2025-10-09
Classification
Cardiovascular
Generic name
Stent graft, bypass, superficial femoral artery
Approval order statement
a manufacturing site located at Endologix, LLC at 3910 Brickway Blvd., Santa Rosa, CA 95403 for manufacturing the TORUS Stent Graft System and associated manufacturing changes and for an alternate contract sterilizer for the TORUS Stent Graft System located at Steris Isomedix Services at 43425 Business Park Drive, Temecula, CA 92590

Current openFDA PMA Record#

Device
DETOUR System
Applicant
Endologix, LLC
PMA number
P220021
Supplement
S006
Product code
QWM
Generic name
Stent graft, bypass, superficial femoral artery
Decision date
2025-10-09
Decision code
APPR
Date received
2025-08-28
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
a manufacturing site located at Endologix, LLC at 3910 Brickway Blvd., Santa Rosa, CA 95403 for manufacturing the TORUS Stent Graft System and associated manufacturing changes and for an alternate contract sterilizer for the TORUS Stent Graft System located at Steris Isomedix Services at 43425 Business Park Drive, Temecula, CA 92590