Russell B. Walther
Country not established
- Devices
- 1
What Russell B. Walther makes
The company manufactures the SPRYTIE surgical devices (models ST001, ST002, and ST003), which are designed for use in orthopedic and spinal procedures. These devices are intended to assist in the precise placement of screws and other fixation hardware during spinal surgery.
The SPRYTIE devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sprytie, Models ST001, ST002 And ST003 Ref K092530
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Russell B. Walther have in the registry?
The registry currently lists 1 device for Russell B. Walther. Devices recorded under merged duplicate company entries are counted once.
Which registries list Russell B. Walther's devices?
Among its 1 most recently registered device, Russell B. Walther has devices listed in FDA 510(k) (1 device).
What risk classes do Russell B. Walther's devices fall under?
Among its 1 most recently registered device, the classes recorded for Russell B. Walther's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Russell B. Walther in the registry?
The most recently registered devices listed for Russell B. Walther include SPRYTIE, MODELS ST001, ST002 AND ST003.