Atlas FDA

OVATIO CRT

FDA premarket approval P060027/S010 · decided 2009-02-23

Approval details

PMA number
P060027
Supplement
S010
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
OVATIO CRT
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
MicroPort CRM USA, Inc.
Date received
2009-01-28
Decision date
2009-02-23
Days to decision
26 days
Decision code
OK30
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
CHANGE IN THE TYPE OF X-RAY MACHINE.

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