Atlas FDA

PARADYM CRT

FDA premarket approval P060027/S034 · decided 2011-12-12

Approval details

PMA number
P060027
Supplement
S034
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
2011-11-10
Decision date
2011-12-12
Days to decision
32 days
Decision code
OK30
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
Arlington, TN
Statement
ALTERNATE EQUIPMENT FOR THE LASER WELDING PROCESS.

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