Atlas FDA

OVATIO CRT-D SYSTEM

FDA premarket approval P060027/S002 · decided 2008-10-31

Approval details

PMA number
P060027
Supplement
S002
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
OVATIO CRT-D SYSTEM
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
MicroPort CRM USA, Inc.
Date received
2008-06-13
Decision date
2008-10-31
Days to decision
140 days
Decision code
APPR
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
APPROVAL OF THE POST-APPROVAL STUDY.

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