Atlas FDA

HeartWare HVAD System

FDA premarket approval P100047/S142 · decided 2020-05-07

Approval details

PMA number
P100047
Supplement
S142
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
HeartWare HVAD System
Generic name
Ventricular (assist) bypass
Applicant
Medtronic
Date received
2019-07-05
Decision date
2020-05-07
Days to decision
307 days
Decision code
APPR
Product code
DSQ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for the design modifications to the monitor AC adapter and labeling modifications to the HVAD Physician IFU and Patient Manual.

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