FDA 510(k)

APTUS 手部舟狀骨板

K 號：K234062 · 2024-03-21

決定日期2024-03-21

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

APTUS Hand Scaphoid Plates is the device name listed in this FDA 510(k) record. The listed applicant is Medartis AG. It received FDA 510(k) clearance on 2024-03-21 under 510(k) number K234062. 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 APTUS Hand Scaphoid Plates?

APTUS Hand Scaphoid Plates is a medical device that received FDA 510(k) clearance on 2024-03-21. The listed applicant is Medartis AG. The 510(k) number is K234062.

When did APTUS Hand Scaphoid Plates receive FDA 510(k) clearance?

APTUS Hand Scaphoid Plates received FDA 510(k) clearance on 2024-03-21, under 510(k) number K234062.

Who is the listed applicant for APTUS Hand Scaphoid Plates?

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

What is the FDA product code for APTUS Hand Scaphoid Plates?

The FDA product code for APTUS Hand Scaphoid Plates is HRS.

其他以 Medartis AG 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。

K260761APTUS 肩胛骨系統 2.8 K260934TITAN指甲針；APTUS K針系統 K253916APTUS Shoulder Proximal Humerus System, PentaLock 3.5 K243610APTUS 手部系統; APTUS 肘部背側桡骨頭板 K240613APTUS 肘部背側桡骨頭板 K232105APTUS 足部系統 2.8-3.5

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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。

K261892ProRib固定系統Costa Surgical, Inc.K262098EnHAnce PEEK 趾骨隆起系統Nvision Biomedical Technologies K262963TMC 偽骨固定系統Treace Medical Concepts, Inc.K261647Tempo植板系統；超壓縮螺釘系統Pace Surgical K261830FRAXION 3.5 板系統（多種 - 見目錄）；FRAXION 4.5 板系統（多種 - 見目錄）；FRAXION Mini 板系統（多種 - 見目錄）；FRAXION 骨釘系統（多種 - 見目錄）Ortler Global Tibbi Gerecler Anonim Sirketi K262537Versalock 無菌板片系統GM Dos Reis Industria e Comercio Ltda.

官方來源

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