Radicle Orthopaedics, Inc. is one of 18477 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radicle Orthopaedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RASL Repair Kit
1
Total
1
Cleared
0
Denied
Radicle Orthopaedics, Inc. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Radicle Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Radicle Orthopaedics, Inc.
1 devices