Ceterix Orthopaedics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceterix Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NovoStitch Pro Meniscal Repair System, CTX-A004 (size 0), NovoStitch Pro Meniscal Repair System
3
Total
3
Cleared
0
Denied
Ceterix Orthopaedics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 3 cleared submissions from 2015 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ceterix Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qrac, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ceterix Orthopaedics, Inc.
3 devices