Stryker Corporate - FDA 510(k) Cleared Devices
Recent clearances: Styrker OrthoMap Express Knee System, Navigated XIA 4.5 Polyaxial Screwdriver, SPINEMASK TRACKER, SPINEMAP 3D 3.0-SOFTWARE,SPINEMAP 3D 3.0-UPGREADE, SPINEMAP 3D 3.0-ENABLE, SPINEMAP 3D 3.0-SALES D
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Corporate Neurology ✕
2 devices