Atlas FDA

PARADYM CRT

FDA premarket approval P060027/S025 · decided 2010-07-09

Approval details

PMA number
P060027
Supplement
S025
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PARADYM CRT
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
MicroPort CRM USA, Inc.
Date received
2010-06-04
Decision date
2010-07-09
Days to decision
35 days
Decision code
OK30
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
CHANGE TO IN-SOURCE THE MICRO-ELECTRONIC ASSEMBLY OF ELECTRONIC HYBRIDE MODULES.

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