FDA 510(k) Applications Submitted by Ceterix Orthopaedics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K143356 11/24/2014 NovoStitch Plus Meniscal Repair System Ceterix Orthopaedics, Inc.
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.


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