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FDA 510(k) Application Details - K211518
Device Classification Name
Catheter, Peripheral, Atherectomy
More FDA Info for this Device
510(K) Number
K211518
Device Name
Catheter, Peripheral, Atherectomy
Applicant
Volcano AtheroMed, Inc.
1530 O'Brien Drive, Suite A
Menlo Park, CA 94025 US
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Contact
Jean Chang
Other 510(k) Applications for this Contact
Regulation Number
870.4875
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Classification Product Code
MCW
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More FDA Info for this Product Code
Date Received
05/17/2021
Decision Date
06/14/2021
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
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