Apogee Orthosolutions
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- Devices
- 1
What Apogee Orthosolutions makes
Apogee Orthosolutions manufactures the Monster Screw System, a surgical fixation device used in orthopedic procedures.
The Monster Screw System is classified as a Class II medical device and is listed in the FDA 510(k) registry. Apogee Orthosolutions is based in the United States. This record supports the listed information.
Catalogue
Monster Screw System Ref K124027
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apogee Orthosolutions have in the registry?
The registry currently lists 1 device for Apogee Orthosolutions. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apogee Orthosolutions's devices?
Among its 1 most recently registered device, Apogee Orthosolutions has devices listed in FDA 510(k) (1 device).
What risk classes do Apogee Orthosolutions's devices fall under?
Among its 1 most recently registered device, the classes recorded for Apogee Orthosolutions's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apogee Orthosolutions in the registry?
The most recently registered devices listed for Apogee Orthosolutions include MONSTER SCREW SYSTEM.