Osteocentric Trauma is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Osteocentric Trauma - FDA 510(k) Cleared Devices
Recent clearances: OsteoCentric Bone Plate and Screw System
1
Total
1
Cleared
0
Denied
Osteocentric Trauma has 1 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteocentric Trauma Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Osteocentric Trauma
1 devices