Atlas FDA

MEDTRONIC COREVALVE(R) EVOLUT R SYSTEM

FDA premarket approval P130021/S022 · decided 2016-08-26

Approval details

PMA number
P130021
Supplement
S022
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
MEDTRONIC COREVALVE(R) EVOLUT R SYSTEM
Generic name
Aortic valve, prosthesis, percutaneously delivered
Applicant
Medtronic, Inc.
Date received
2016-06-21
Decision date
2016-08-26
Days to decision
66 days
Decision code
APPR
Product code
NPT
Advisory committee
Cardiovascular
Expedited review
No
Location
Miinneapolis, MN
Statement
Approval for modifying the dimensions of the screw gear component.

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510(k) clearances by this applicant

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