Atlas FDA

VARIOUS FAMILIES OF ICDS

FDA premarket approval P980016/S182 · decided 2009-03-24

Approval details

PMA number
P980016
Supplement
S182
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
VARIOUS FAMILIES OF ICDS
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Medtronic Cardiac Rhythm Disease Management
Date received
2009-02-23
Decision date
2009-03-24
Days to decision
29 days
Decision code
OK30
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
TRANSFER OF PROCESSES TO A CONTRACT MANUFACTURING FACILITY.

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