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FDA 510(k) Application Details - K231848
Device Classification Name
More FDA Info for this Device
510(K) Number
K231848
Device Name
Triever20 Curve (21-201)
Applicant
Inari Medical, Inc.
6001 Oak Canyon
Suite 100
Irvine, CA 92618 US
Other 510(k) Applications for this Company
Contact
Anthony Lam
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
QEW
Other 510(k) Applications for this Device
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Date Received
06/23/2023
Decision Date
07/21/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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