FDA 510(k) Applications Submitted by Tarhan Kayihan

FDA 510(k) Number Submission Date Device Name Applicant
K180531 02/28/2018 NovoStitch Pro Meniscal Repair System Ceterix Orthopaedics, Inc.
K181772 07/03/2018 NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0) Ceterix Orthopaedics, Inc.
K052019 07/26/2005 NORTH COAST BUFFERED IONTOPHORESIS ELECTRODE NORTH COAST MEDICAL, INC.


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