Class Class II

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 (K212194)

K212194 2023-02-16 Traditional
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Description

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 by Stryker Corporation — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK212194
Clearance Date2023-02-16
Clearance TypeTraditional
Product CodeHAW
Regulation Number882.4560

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