Atlas FDA

POWERLINK SYSTEM

FDA premarket approval P040002/S002 · decided 2006-02-08

Approval details

PMA number
P040002
Supplement
S002
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
POWERLINK SYSTEM
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Endologix, LLC
Date received
2005-11-10
Decision date
2006-02-08
Days to decision
90 days
Decision code
APPR
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
APPROVAL FOR A MANUFACTURING SITE IN IRVINE, CALIFORNIA.

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