Integra Spine (Integra Lifesciences)
Country not established
- Devices
- 1
What Integra Spine (Integra Lifesciences) makes
Integra Spine manufactures lateral fusion devices designed for spinal stabilization procedures, including systems for interbody fusion in the lumbar and cervical regions.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Lateral Fusion Device Ref K112986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integra Spine (Integra Lifesciences) have in the registry?
The registry currently lists 1 device for Integra Spine (Integra Lifesciences). Devices recorded under merged duplicate company entries are counted once.
Which registries list Integra Spine (Integra Lifesciences)'s devices?
Among its 1 most recently registered device, Integra Spine (Integra Lifesciences) has devices listed in FDA 510(k) (1 device).
What risk classes do Integra Spine (Integra Lifesciences)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Integra Spine (Integra Lifesciences)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integra Spine (Integra Lifesciences) in the registry?
The most recently registered devices listed for Integra Spine (Integra Lifesciences) include LATERAL FUSION DEVICE.