Integrity Spine Lumbar Interbody Fusion System
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- Devices
- 1
What Integrity Spine Lumbar Interbody Fusion System makes
The company manufactures the Integrity Spine Lumbar Interbody Fusion System, a device designed for lumbar spinal fusion procedures to stabilize the spine and promote bone growth between vertebrae.
This product is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Integrity Spine Lumbar Interbody Fusion System Ref K151819
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Integrity Spine Lumbar Interbody Fusion System have in the registry?
The registry currently lists 1 device for Integrity Spine Lumbar Interbody Fusion System. Devices recorded under merged duplicate company entries are counted once.
Which registries list Integrity Spine Lumbar Interbody Fusion System's devices?
Among its 1 most recently registered device, Integrity Spine Lumbar Interbody Fusion System has devices listed in FDA 510(k) (1 device).
What risk classes do Integrity Spine Lumbar Interbody Fusion System's devices fall under?
Among its 1 most recently registered device, the classes recorded for Integrity Spine Lumbar Interbody Fusion System's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Integrity Spine Lumbar Interbody Fusion System in the registry?
The most recently registered devices listed for Integrity Spine Lumbar Interbody Fusion System include Integrity Spine Lumbar Interbody Fusion System.