Stryker Leibinger GmbH & Co. Kg - Navigation
GermanyFDA applicant, unverified
- Devices
- 1
What Stryker Leibinger GmbH & Co. Kg - Navigation makes
Stryker Leibinger GmbH & Co. KG - Navigation develops the NavSuite3 Kit, a surgical navigation system designed for precise intraoperative guidance in orthopedic and spinal procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the U.S. regulatory database. The entity operates with a base in the United States.
Catalogue
NavSuite3 Kit Ref K150301
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Leibinger GmbH & Co. KG - Navigation have in the registry?
The registry currently lists 1 device for Stryker Leibinger GmbH & Co. KG - Navigation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Leibinger GmbH & Co. KG - Navigation's devices?
Among its 1 most recently registered device, Stryker Leibinger GmbH & Co. KG - Navigation has devices listed in FDA 510(k) (1 device).
What risk classes do Stryker Leibinger GmbH & Co. KG - Navigation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stryker Leibinger GmbH & Co. KG - Navigation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Leibinger GmbH & Co. KG - Navigation in the registry?
The most recently registered devices listed for Stryker Leibinger GmbH & Co. KG - Navigation include NavSuite3 Kit.