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FDA 510(k)

T2 Alpha Femur Retrograde Nailing System

K 號:K250163 · 2025-08-13

申請人Stryker GmbH
決定日期2025-08-13
產品代碼HSB
諮詢委員會或
決定相當於

器材摘要

T2 Alpha Femur Retrograde Nailing 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 2025-08-13 under 510(k) number K250163. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the T2 Alpha Femur Retrograde Nailing System?

T2 Alpha Femur Retrograde Nailing System is a medical device that received FDA 510(k) clearance on 2025-08-13. The listed applicant is Stryker GmbH. The 510(k) number is K250163.

When did T2 Alpha Femur Retrograde Nailing System receive FDA 510(k) clearance?

T2 Alpha Femur Retrograde Nailing System received FDA 510(k) clearance on 2025-08-13, under 510(k) number K250163.

Who is the listed applicant for T2 Alpha Femur Retrograde Nailing 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 T2 Alpha Femur Retrograde Nailing System?

The FDA product code for T2 Alpha Femur Retrograde Nailing System is HSB.

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其他以 Stryker GmbH 為申請人之記錄

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相關器械(代碼:HSB)

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