Atlas FDA

ESSURE SYSTEM

FDA premarket approval P020014/S045 · decided 2016-04-28

Approval details

PMA number
P020014
Supplement
S045
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
ESSURE SYSTEM
Generic name
Transcervical contraceptive tubal occlusion device
Applicant
Bayer Pharma AG
Date received
2016-02-25
Decision date
2016-04-28
Days to decision
63 days
Decision code
APPR
Product code
HHS
Advisory committee
Obstetrics/Gynecology
Expedited review
No
Location
Berlin
Statement
Approval for modifications to the post-approval study protocol.

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