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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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