Innospine, Inc.
Country not established
- Devices
- 1
What Innospine, Inc. makes
Innospine, Inc. manufactures diagnostic systems for spinal interventions, including the Functional Anaesthetic Discography (FAD) System. This comprises a catheter kit and an introducer needle designed to assess spinal disc function under anaesthetic conditions.
The FAD System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Functional Anaesthetic Discography (Fad) System, Including Fad Catheter Kit And Fad Introducer Needle Ref K043500
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innospine, Inc. have in the registry?
The registry currently lists 1 device for Innospine, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innospine, Inc.'s devices?
Among its 1 most recently registered device, Innospine, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Innospine, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Innospine, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Innospine, Inc. in the registry?
The most recently registered devices listed for Innospine, Inc. include FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) SYSTEM, INCLUDING FAD CATHETER KIT AND FAD INTRODUCER NEEDLE.