Porosteon, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Porosteon, Inc. makes
Porosteon, Inc. produces the POROSTEON PHUSION METAL CERVICAL CAGE, a medical device used in spinal surgery.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Porosteon Phusion Metal Cervical Cage Ref K142041
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porosteon, Inc. have in the registry?
The registry currently lists 1 device for Porosteon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porosteon, Inc.'s devices?
Among its 1 most recently registered device, Porosteon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Porosteon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Porosteon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porosteon, Inc. in the registry?
The most recently registered devices listed for Porosteon, Inc. include POROSTEON PHUSION METAL CERVICAL CAGE.