Atlas FDA

Hancock II Bioprosthesis

FDA premarket approval P970031/S070 · decided 2023-08-10

Approval details

PMA number
P970031
Supplement
S070
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Hancock II Bioprosthesis
Generic name
heart-valve, non-allograft tissue
Applicant
Medtronic, Inc.
Date received
2023-07-31
Decision date
2023-08-10
Days to decision
10 days
Decision code
OK30
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Ana, CA
Statement
Manufacturing site addition for the supplier of the primary packaging component for the Mosaic, Freestyle, Hancock II, and Avalus bioprostheses.

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