FDA 510(k) Applications Submitted by Surmodics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K192814 10/01/2019 Pounce Thrombus Retrieval System Surmodics, Inc.
K211492 05/13/2021 Pounce Thrombectomy System Surmodics, Inc.
K190644 03/13/2019 Guide Sheath Surmodics, Inc.
K231828 06/21/2023 PounceÖ Sheath Surmodics, Inc.
K173560 11/17/2017 Microcatheter Surmodics, Inc.


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