Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K211013
Device Classification Name
More FDA Info for this Device
510(K) Number
K211013
Device Name
FlowTriever Retrieval/Aspiration System, FlowTriever Catheters, Triever 16, Triever 20, Triever 20 Curve, Triever 24
Applicant
Inari Medical, Inc.
9 Parker, Suite 100
Irvine, CA 92618 US
Other 510(k) Applications for this Company
Contact
Larry Boucher
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
More FDA Info for this Product Code
Date Received
04/05/2021
Decision Date
04/30/2021
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
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact