FDA 510(k) Applications Submitted by Kurtis Hunsberger

FDA 510(k) Number Submission Date Device Name Applicant
K200095 01/16/2020 Streamline Navigated Instruments Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc.
K150186 01/27/2015 Chariot Guiding Sheath BOSTON SCIENTIFIC CORP.
K140641 03/12/2014 VESSIX GUIDE SHEATH 7F, 45 CM, RDC, VESSIX GUIDE SHEATH 7F, 45CM, LIMA Boston Scientific Corporation
K152401 08/25/2015 Stingray LP Catheter BOSTON SCIENTIFIC CORPORATION
K192800 09/30/2019 Streamline TL Spinal Fixation System Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.)


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