W.D. Renner Consulting Co.
Country not established
- Devices
- 1
What W.D. Renner Consulting Co. makes
W.D. Renner Consulting Co. develops the RENNER-PLAN, a medical device designed for surgical planning and pre-operative assessment, likely used in orthopedic or spinal procedures to aid in treatment strategies.
The RENNER-PLAN is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Renner-Plan Ref K894722
510(k) 510(k)
Frequently asked questions
How many devices does W.D. Renner Consulting Co. have in the registry?
The registry currently lists 1 device for W.D. Renner Consulting Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list W.D. Renner Consulting Co.'s devices?
Among its 1 most recently registered device, W.D. Renner Consulting Co. has devices listed in FDA 510(k) (1 device).
What risk classes do W.D. Renner Consulting Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for W.D. Renner Consulting Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from W.D. Renner Consulting Co. in the registry?
The most recently registered devices listed for W.D. Renner Consulting Co. include RENNER-PLAN.