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FDA 510(k)

正骨科導向精準膝軟體；正骨科導向快遞膝軟體；正骨科導向多功能臀部軟體；Q導向系統

K 號：K233542 · 2024-03-14

申請人Stryker Leibinger GmbH & Co KG
決定日期2024-03-14
產品代碼OLO
諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)
決定相當於

器材摘要

Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2024-03-14 under 510(k) number K233542. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System?

Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System is a medical device that received FDA 510(k) clearance on 2024-03-14. The listed applicant is Stryker Leibinger GmbH & Co KG. The 510(k) number is K233542.

When did Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System receive FDA 510(k) clearance?

Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System received FDA 510(k) clearance on 2024-03-14, under 510(k) number K233542.

Who is the listed applicant for Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System?

The FDA 510(k) record lists Stryker Leibinger GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System?

The FDA product code for Ortho Guidance Precision Knee Software; Ortho Guidance Express Knee Software; Ortho Guidance Versatile Hip Software; Q Guidance System is OLO.

相關臨床試驗

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Stryker Leibinger GmbH & Co KG 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K261054肋骨板系統K254233醫用設備規範文本翻譯： MEDPOR客製化植入套件K253623脊椎導引 5.4 軟體；脊椎導引 5.4 升級；脊椎導引 5.4 更新；脊椎導引 5.4 軟體啟用；脊椎導引 5.4 買賣展示；Q 閼钻追踪器；NavLock 适配器；Elite Q 附件；Elite 切割附件；Maestro 空氣馬達K252871脊椎導引 5.3 軟體；Q 間體儀器；Elite Q 附件；Elite 切割附件K243491胸骨板擴張K241517Q導向系統；Mako脊椎系統；

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相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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