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FDA 510(k)

Stryker 骨科醫療設備標籤更新

K 號:K243784 · 2025-02-06

決定日期2025-02-06
產品代碼LPH
諮詢委員會或
決定相當於

器材摘要

Stryker Orthopaedics Hip Devices Labeling Update is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2025-02-06 under 510(k) number K243784. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Stryker Orthopaedics Hip Devices Labeling Update?

Stryker Orthopaedics Hip Devices Labeling Update is a medical device that received FDA 510(k) clearance on 2025-02-06. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K243784.

When did Stryker Orthopaedics Hip Devices Labeling Update receive FDA 510(k) clearance?

Stryker Orthopaedics Hip Devices Labeling Update received FDA 510(k) clearance on 2025-02-06, under 510(k) number K243784.

Who is the listed applicant for Stryker Orthopaedics Hip Devices Labeling Update?

The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stryker Orthopaedics Hip Devices Labeling Update?

The FDA product code for Stryker Orthopaedics Hip Devices Labeling Update is LPH.

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其他以 Howmedica Osteonics Corp., Dba Stryker Orthopaedics 為申請人之記錄

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相關器械(代碼:LPH)

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官方來源

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