Praxim Medivision, SA
FranceFDA applicant, unverified
- Devices
- 2
What Praxim Medivision, SA makes
Praxim Medivision, SA designs and manufactures computer-assisted surgical navigation systems for orthopedic procedures, including total knee surgeries with integrated tracking blocks and CT-based navigation solutions.
Their products are classified as Class II medical devices and are authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ctlogics Navigations Systems Ref K063408
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Praxim Medivision, SA have in the registry?
The registry currently lists 2 devices for Praxim Medivision, SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Praxim Medivision, SA's devices?
Among its 2 most recently registered devices, Praxim Medivision, SA has devices listed in FDA 510(k) (2 devices).
What risk classes do Praxim Medivision, SA's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Praxim Medivision, SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Praxim Medivision, SA in the registry?
The most recently registered devices listed for Praxim Medivision, SA include TOTAL KNEE SURGETICS NAVIGATION SYSTEM WITH IBLOCK and CTLOGICS NAVIGATIONS SYSTEMS.