University of Utah/School of Medicine
Country not established
- Devices
- 1
What University of Utah/School of Medicine makes
The University of Utah/School of Medicine develops orthopedic fixation devices, including the Growth Guidance Plate, designed to manage skeletal growth and alignment in pediatric patients.
This device is classified as Class II under FDA regulations and is supported by a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Growth Guidance Plate Ref K031493
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does University of Utah/School of Medicine have in the registry?
The registry currently lists 1 device for University of Utah/School of Medicine. Devices recorded under merged duplicate company entries are counted once.
Which registries list University of Utah/School of Medicine's devices?
Among its 1 most recently registered device, University of Utah/School of Medicine has devices listed in FDA 510(k) (1 device).
What risk classes do University of Utah/School of Medicine's devices fall under?
Among its 1 most recently registered device, the classes recorded for University of Utah/School of Medicine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from University of Utah/School of Medicine in the registry?
The most recently registered devices listed for University of Utah/School of Medicine include GROWTH GUIDANCE PLATE.