Medartis Medizinprodukte Und Forschung AG
GermanyFDA applicant, unverified
- Devices
- 1
What Medartis Medizinprodukte Und Forschung AG makes
Medartis produces orthopedic surgical devices, including the SYNTHACER and SYNTRICER systems, which are designed for bone fixation and stabilization in joint replacement procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Synthacer; Syntricer Ref K041177
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medartis Medizinprodukte Und Forschung AG have in the registry?
The registry currently lists 1 device for Medartis Medizinprodukte Und Forschung AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medartis Medizinprodukte Und Forschung AG's devices?
Among its 1 most recently registered device, Medartis Medizinprodukte Und Forschung AG has devices listed in FDA 510(k) (1 device).
What risk classes do Medartis Medizinprodukte Und Forschung AG's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medartis Medizinprodukte Und Forschung AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medartis Medizinprodukte Und Forschung AG in the registry?
The most recently registered devices listed for Medartis Medizinprodukte Und Forschung AG include SYNTHACER; SYNTRICER.