Biomet Spine & Bone Healing Technologies
Country not established
- Devices
- 1
What Biomet Spine & Bone Healing Technologies makes
Biomet Spine & Bone Healing Technologies makes spinal implant systems, specifically the SOLITARIE PEEK ANTERIOR SPINAL SYSTEM, which is intended to be called COLITAIRE 35.
The device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomet Spine & Bone Healing Technologies have in the registry?
The registry currently lists 1 device for Biomet Spine & Bone Healing Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Spine & Bone Healing Technologies's devices?
Among its 1 most recently registered device, Biomet Spine & Bone Healing Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Biomet Spine & Bone Healing Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Biomet Spine & Bone Healing Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomet Spine & Bone Healing Technologies in the registry?
The most recently registered devices listed for Biomet Spine & Bone Healing Technologies include SOLITARIE PEEK ANTERIOR SPINAL SYSTEM-TO BE CALLED COLITAIRE 35.