Musculoskeletal Clinical Regulatory Advisers
Country not established
- Devices
- 1
What Musculoskeletal Clinical Regulatory Advisers makes
The company designs and manufactures the VU CPOD intervertebral body fusion device, a spinal implant used for stabilizing and fusing vertebrae in the cervical or lumbar spine during surgical procedures.
This device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company operates from the United States.
Catalogue
Vu Cpod Intervertebral Bodu Fusion Device Ref K101363
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Musculoskeletal Clinical Regulatory Advisers have in the registry?
The registry currently lists 1 device for Musculoskeletal Clinical Regulatory Advisers. Devices recorded under merged duplicate company entries are counted once.
Which registries list Musculoskeletal Clinical Regulatory Advisers's devices?
Among its 1 most recently registered device, Musculoskeletal Clinical Regulatory Advisers has devices listed in FDA 510(k) (1 device).
What risk classes do Musculoskeletal Clinical Regulatory Advisers's devices fall under?
Among its 1 most recently registered device, the classes recorded for Musculoskeletal Clinical Regulatory Advisers's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Musculoskeletal Clinical Regulatory Advisers in the registry?
The most recently registered devices listed for Musculoskeletal Clinical Regulatory Advisers include VU CPOD INTERVERTEBRAL BODU FUSION DEVICE.