Stryker Cmf
Country not established
- Devices
- 2
What Stryker Cmf makes
Stryker Cmf manufactures injectable bone cement, used for spinal and orthopedic procedures, and external fixation systems for stabilizing fractures and deformities. These products are designed to provide structural support and promote bone healing in surgical settings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Stryker Injectable Cement Ref K060750
Regimes: 510(k) Registry: 510(k)Stryker External Fixation System Ref K071628
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Cmf have in the registry?
The registry currently lists 2 devices for Stryker Cmf. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Cmf's devices?
Among its 2 most recently registered devices, Stryker Cmf has devices listed in FDA 510(k) (2 devices).
What risk classes do Stryker Cmf's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stryker Cmf's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Cmf in the registry?
The most recently registered devices listed for Stryker Cmf include STRYKER INJECTABLE CEMENT and STRYKER EXTERNAL FIXATION SYSTEM.