Atlas FDA

PARADYM CRT-D, RF CRT-D

FDA premarket approval P060027/S040 · decided 2012-06-11

Approval details

PMA number
P060027
Supplement
S040
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PARADYM CRT-D, RF CRT-D
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
MicroPort CRM USA, Inc.
Date received
2012-05-16
Decision date
2012-06-11
Days to decision
26 days
Decision code
OK30
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
ALTERNATE MANUFACTURING EQUIPMENT.

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