FDA 510(k) Applications Submitted by Jennifer Mrkvicka

FDA 510(k) Number Submission Date Device Name Applicant
K201170 05/01/2020 Athletis PTA Balloon Dilatation Catheter Boston Scientific Corporation
K231891 06/27/2023 Virtue Male Sling System with Alexis Wound Retractor Convenience Kit Coloplast
K242473 08/20/2024 Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562) Coloplast Corp


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