Atlas FDA

POWERLINK SYSTEM

FDA premarket approval P040002/S003 · decided 2006-02-01

Approval details

PMA number
P040002
Supplement
S003
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
POWERLINK SYSTEM
Generic name
SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
Applicant
Endologix, LLC
Date received
2006-01-10
Decision date
2006-02-01
Days to decision
22 days
Decision code
OK30
Product code
MIH
Advisory committee
Cardiovascular
Expedited review
No
Location
Irvine, CA
Statement
SWITCH FROM TWO-PART EPOXY REQUIRING 48-HOUR CURE TIME TO TWO-PART EPOXY REQUIRING 1-HOUR CURE TIME.

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