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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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