Renaissance Instruments, LLC
Country not established
- Devices
- 1
What Renaissance Instruments, LLC makes
Renaissance Instruments, LLC manufactures the FS 1000 Knee System, a medical device designed for knee joint replacement or reconstruction procedures.
The FS 1000 Knee System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fs 1000 Knee System Ref K991052
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Renaissance Instruments, LLC have in the registry?
The registry currently lists 1 device for Renaissance Instruments, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renaissance Instruments, LLC's devices?
Among its 1 most recently registered device, Renaissance Instruments, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Renaissance Instruments, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Renaissance Instruments, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Renaissance Instruments, LLC in the registry?
The most recently registered devices listed for Renaissance Instruments, LLC include FS 1000 KNEE SYSTEM.