Atlas FDA

Avalus Bioprosthesis

FDA premarket approval P170006/S018 · decided 2020-10-22

Approval details

PMA number
P170006
Supplement
S018
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
Avalus Bioprosthesis
Generic name
heart-valve, non-allograft tissue
Applicant
Medtronic, Inc.
Date received
2020-10-02
Decision date
2020-10-22
Days to decision
20 days
Decision code
APPR
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Ana, CA
Statement
Approval for an updated protocol and additional testing performed for shelf-life extension.

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