Atlas FDA

Avalus Bioprosthesis

FDA premarket approval P170006/S020 · decided 2022-03-01

Approval details

PMA number
P170006
Supplement
S020
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Avalus Bioprosthesis
Generic name
heart-valve, non-allograft tissue
Applicant
Medtronic, Inc.
Date received
2022-02-28
Decision date
2022-03-01
Days to decision
1 days
Decision code
OK30
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Ana, CA
Statement
Use of a new data management system for microbiology laboratory test data and data reporting at the Medtronic Tijuana facility for the Evolut R, Evolut PRO, Evolut PRO+, and Evolut FX Transcatheter Aortic Valves (TAVs), Harmony and Melody Transcatheter Pulmonic Valves (TPV), and Avalus bioprosthesis products.

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