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FREESTYLE AORTIC ROOT BIOPROSTHESIS

FDA premarket approval P970031/S043 · decided 2013-07-30

Approval details

PMA number
P970031
Supplement
S043
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
FREESTYLE AORTIC ROOT BIOPROSTHESIS
Generic name
heart-valve, non-allograft tissue
Applicant
Medtronic, Inc.
Date received
2013-07-01
Decision date
2013-07-30
Days to decision
29 days
Decision code
OK30
Product code
LWR
Advisory committee
Cardiovascular
Expedited review
No
Location
Santa Ana, CA
Statement
NEWLY CONSTRUCTED CONTROLLED ENVIRONMENT AREA (CEA) AT THE MANUFACTURING FACILITY IN SANTA ANA, CA.

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