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FDA premarket approval P900061/S137 · decided 2015-10-02

Approval details

PMA number
P900061
Supplement
S137
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
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Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Medtronic Cardiac Rhythm Disease Management
Date received
2015-09-10
Decision date
2015-10-02
Days to decision
22 days
Decision code
OK30
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
IMPLEMENTATION OF NEW SERIAL NUMBER PRINTING SOFTWARE WITHIN THE EXISTING TRACEABILITY SYSTEM.

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