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ENDOLOGIX POWERLINK SYSTEM

FDA premarket approval P040002/S005 · decided 2006-05-17

Approval details

PMA number
P040002
Supplement
S005
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
ENDOLOGIX POWERLINK SYSTEM
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Endologix, LLC
Date received
2006-03-20
Decision date
2006-05-17
Days to decision
58 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR A NEW VERSION OF THE VISIFLEX DELIVERY CATHETER FOR BOTH THE BIFURCATED AND STRAIGHT STENT GRAFTS.

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