Arent, Fox, Kintner, Plotkin & Kahn
Country not established
- Devices
- 1
What Arent, Fox, Kintner, Plotkin & Kahn makes
The company manufactures the CIMPAT N, a medical device designed for use in spinal surgery to facilitate bone fusion and stabilization.
The device portfolio is regulated under FDA Class II and requires 510(k) clearance. The company is based in the United States.
Catalogue
Cimpat N Ref K972485
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arent, Fox, Kintner, Plotkin & Kahn have in the registry?
The registry currently lists 1 device for Arent, Fox, Kintner, Plotkin & Kahn. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arent, Fox, Kintner, Plotkin & Kahn's devices?
Among its 1 most recently registered device, Arent, Fox, Kintner, Plotkin & Kahn has devices listed in FDA 510(k) (1 device).
What risk classes do Arent, Fox, Kintner, Plotkin & Kahn's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arent, Fox, Kintner, Plotkin & Kahn's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arent, Fox, Kintner, Plotkin & Kahn in the registry?
The most recently registered devices listed for Arent, Fox, Kintner, Plotkin & Kahn include CIMPAT N.