FDA 510(k) Application Details - K211697

Device Classification Name Catheter, Thrombus Retriever

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510(K) Number K211697
Device Name Catheter, Thrombus Retriever
Applicant Wallaby Medical
22901 Mill Creek Drive
Laguna Hills, CA 92653 US
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Contact Nathaniel Knock
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Regulation Number 870.1250

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Classification Product Code NRY
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Date Received 06/03/2021
Decision Date 11/16/2021
Decision SESE - SUBST EQUIV
Classification Advisory Committee CV - Cardiovascular
Review Advisory Committee NE - Neurology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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