Atlas FDA

Mosaic Bioprosthesis

FDA premarket approval P990064/S093 · decided 2025-11-10

Approval details

PMA number
P990064
Supplement
S093
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Mosaic Bioprosthesis
Generic name
replacement Heart-valve
Applicant
Medtronic, Inc.
Date received
2025-08-13
Decision date
2025-11-10
Days to decision
89 days
Decision code
APPR
Product code
DYE
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Ana, CA
Statement
Approval for implementation of updates to the product labels and IFUs, and the implementation of a new temperature indicator on the secondary package shelf cartons for the Mosaic, Hancock II, Avalus, and Freestyle bioprostheses

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