Stryker Corporation - FDA 510(k) Cleared Devices
Recent clearances: Connected OR Hub with Device and Voice Control, SDC4K Information Management System with Device and Voice Control, Stryker Q Guidance System with Cranial Guidance Software, CranialMask Tracker and Microscope Tracker, Passive Optical Navigation Instruments, Mayfield Base with Articulating Arm, and Navigated Biopsy Needle, Electromagnetic Navigation Instruments, Precision Targeting System, Sonopet 1Q 3 7cm 1Q Large
81
Total
81
Cleared
0
Denied
FDA 510(k) Regulatory Record - Stryker Corporation Radiology ✕
1 devices