Prism Surgical Design Pty, Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Aurora® Anterior Lumbar Plate Sytstem Ref K201079
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prism Surgical Design Pty, Ltd. have in the registry?
The registry currently lists 1 device for Prism Surgical Design Pty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prism Surgical Design Pty, Ltd.'s devices?
Among its 1 most recently registered device, Prism Surgical Design Pty, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Prism Surgical Design Pty, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Prism Surgical Design Pty, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prism Surgical Design Pty, Ltd. in the registry?
The most recently registered devices listed for Prism Surgical Design Pty, Ltd. include Aurora® Anterior Lumbar Plate Sytstem.