Arthronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Futura Texture-Trakked Total Hip Stem Ref K921382
Regimes: 510(k) Registry: 510(k)Logyk Acetabular Component System Ref K931107
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthronics, Inc. have in the registry?
The registry currently lists 2 devices for Arthronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthronics, Inc.'s devices?
Among its 2 most recently registered devices, Arthronics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Arthronics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arthronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthronics, Inc. in the registry?
The most recently registered devices listed for Arthronics, Inc. include FUTURA TEXTURE-TRAKKED TOTAL HIP STEM and LOGYK ACETABULAR COMPONENT SYSTEM.