Prism Surgical Design Pty , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Prism Surgical Design Pty , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Aurora® Anterior Lumbar Plate Sytstem
1
Total
1
Cleared
0
Denied
Prism Surgical Design Pty , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Milton, AU.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Prism Surgical Design Pty , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Prism Surgical Design Pty , Ltd.
1 devices