Altiva Corp.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Arctec Semirigid Plating System Ref K051044
Regimes: 510(k) Registry: 510(k)Altiva Classic Acp System Ref K070891
Regimes: 510(k) Registry: 510(k)Hydralok System Ref K051216
Regimes: 510(k) Registry: 510(k)Altes Buttress Plating System Ref K061482
Regimes: 510(k) Registry: 510(k)Contour Ii Spinal System Ref K053070
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Altiva Corp. have in the registry?
The registry currently lists 5 devices for Altiva Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altiva Corp.'s devices?
Among its 5 most recently registered devices, Altiva Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Altiva Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Altiva Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altiva Corp. in the registry?
The most recently registered devices listed for Altiva Corp. include ARCTEC SEMIRIGID PLATING SYSTEM, ALTIVA CLASSIC ACP SYSTEM, HYDRALOK SYSTEM and ALTES BUTTRESS PLATING SYSTEM.