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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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