Jointpoint, Inc. is one of 19157 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Jointpoint, Inc. has 1 FDA 510(k) cleared medical devices. Based in Largo, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Jointpoint, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Musculoskeletal Clinical Regulatory Advisers, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Jointpoint, Inc.
1 devices