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FDA 510(k)

Atlas™ 肱骨釘系統

K 號:K241484 · 2024-11-05

決定日期2024-11-05
產品代碼HSB
諮詢委員會或
決定相當於

器材摘要

Atlas™ Humeral Nail System is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Designs North America, Inc. (Odi-Na). It received FDA 510(k) clearance on 2024-11-05 under 510(k) number K241484. 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 Atlas™ Humeral Nail System?

Atlas™ Humeral Nail System is a medical device that received FDA 510(k) clearance on 2024-11-05. The listed applicant is Orthopedic Designs North America, Inc. (Odi-Na). The 510(k) number is K241484.

When did Atlas™ Humeral Nail System receive FDA 510(k) clearance?

Atlas™ Humeral Nail System received FDA 510(k) clearance on 2024-11-05, under 510(k) number K241484.

Who is the listed applicant for Atlas™ Humeral Nail System?

The FDA 510(k) record lists Orthopedic Designs North America, Inc. (Odi-Na) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Atlas™ Humeral Nail System?

The FDA product code for Atlas™ Humeral Nail System is HSB.

相關臨床試驗

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相關器械(代碼:HSB)

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。

官方來源

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