Stryker Corporate
Country not established
- Devices
- 6
What Stryker Corporate makes
Stryker Corporate manufactures a range of orthopedic and neurosurgical devices, including the PROFESS software suite and suction instruments, the Navigated XIA 4.5 polyaxial screwdriver, the OrthoMap Express knee system, the SPINEMASK tracker and associated SPINEMAP 3D software modules, the NAV3I platform, and the Cranial MAP neuro system.
All of these devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Navigated XIA 4.5 Polyaxial Screwdriver Ref K143597
Regimes: 510(k) Registry: 510(k)Styrker OrthoMap Express Knee System Ref K153240
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Stryker NAV3I Platform Ref K130874
Regimes: 510(k) Registry: 510(k)Cranial Map Neuro Ref K131214
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Corporate have in the registry?
The registry currently lists 6 devices for Stryker Corporate. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Corporate's devices?
Among its 6 most recently registered devices, Stryker Corporate has devices listed in FDA 510(k) (6 devices).
What risk classes do Stryker Corporate's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Stryker Corporate's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Corporate in the registry?
The most recently registered devices listed for Stryker Corporate include PROFESS SOFTWARE, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 70 (DEGREES) SUCTION, PROFESS CURVED 90 (DEGREES), Navigated XIA 4.5 Polyaxial Screwdriver, Styrker OrthoMap Express Knee System and SPINEMASK TRACKER, SPINEMAP 3D 3.0-SOFTWARE, SPINEMAP 3D 3.0-UPGREADE, SPINEMAP 3D 3.0-ENABLE, SPINEMAP 3D 3.0-SALES D.