ストライカーQガイドランスシステムおよび頭蓋ガイドソフトウェア、CranialMask Trackerおよび顕微鏡Tracker、パッシブ光学的ナビゲーション機器、Mayfieldベースおよび可動アーム、ナビゲートバイオプシー針、電磁ナビゲーション機器、精度ターゲティングシステム

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 is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Stryker Corporation. The 510(k) number is K212194.

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 received FDA 510(k) clearance on 2023-02-16, under 510(k) number K212194.

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

The FDA product code for 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 is HAW.