Metasurg
Country not established
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Metasurg Digifuse Implant Ref K111536
Regimes: 510(k) Registry: 510(k)Metasurg Subtalar Implant Ref K111265
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Metasurg Nitinol Staple Implant Ref K123926
Regimes: 510(k) Registry: 510(k)Metasurg Subtalar Implant Ref K070441
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metasurg have in the registry?
The registry currently lists 5 devices for Metasurg. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metasurg's devices?
Among its 5 most recently registered devices, Metasurg has devices listed in FDA 510(k) (5 devices).
What risk classes do Metasurg's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Metasurg's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metasurg in the registry?
The most recently registered devices listed for Metasurg include METASURG DIGIFUSE IMPLANT, METASURG SUBTALAR IMPLANT, METASURG CANNULATED TIATANIUM HEMI IMPLANT, MODEL HM-1000 and METASURG NITINOL STAPLE IMPLANT.