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MICRA TRANSCATHETER PACEMAKER SYSTEM

FDA premarket approval P150033/S012 · decided 2017-06-09

Approval details

PMA number
P150033
Supplement
S012
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MICRA TRANSCATHETER PACEMAKER SYSTEM
Generic name
Leadless pacemaker
Applicant
Medtronic, Inc.
Date received
2016-11-16
Decision date
2017-06-09
Days to decision
205 days
Decision code
APPR
Product code
PNJ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for hardware, firmware, labeling, and manufacturing changes to support replacing the Bluetooth (BT) Classic module with a BT Low Energy module in the monitor base station.

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