FDA 510(k)

PeriPRO™ 髋骨系統，可變角度固定系統，AxSOS 3Ti，Stryker 鍛造系統

K 號：K222381 · 2023-04-27

決定日期2023-04-27

產品代碼HRS

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決定相當於

器材摘要

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker GmbH. It received FDA 510(k) clearance on 2023-04-27 under 510(k) number K222381. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System is a medical device that received FDA 510(k) clearance on 2023-04-27. The listed applicant is Stryker GmbH. The 510(k) number is K222381.

When did PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System receive FDA 510(k) clearance?

PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System received FDA 510(k) clearance on 2023-04-27, under 510(k) number K222381.

Who is the listed applicant for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?

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

What is the FDA product code for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System?

The FDA product code for PeriPRO™ Femur System, Variable Angle Fixation System, AxSOS 3Ti, Stryker Plating System is HRS.

其他以 Stryker GmbH 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。

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相關器械（代碼：HRS）

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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