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FDA 510(k)

sagAlign 腰椎籠架系統(各種型號)

K 號:K241413 · 2024-07-17

決定日期2024-07-17
產品代碼MAX
諮詢委員會或
決定相當於

器材摘要

sagAlign Lumbar Cage System (Various PNs) is the device name listed in this FDA 510(k) record. The listed applicant is Acuity Surgical Devices, LLC. It received FDA 510(k) clearance on 2024-07-17 under 510(k) number K241413. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the sagAlign Lumbar Cage System (Various PNs)?

sagAlign Lumbar Cage System (Various PNs) is a medical device that received FDA 510(k) clearance on 2024-07-17. The listed applicant is Acuity Surgical Devices, LLC. The 510(k) number is K241413.

When did sagAlign Lumbar Cage System (Various PNs) receive FDA 510(k) clearance?

sagAlign Lumbar Cage System (Various PNs) received FDA 510(k) clearance on 2024-07-17, under 510(k) number K241413.

Who is the listed applicant for sagAlign Lumbar Cage System (Various PNs)?

The FDA 510(k) record lists Acuity Surgical Devices, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for sagAlign Lumbar Cage System (Various PNs)?

The FDA product code for sagAlign Lumbar Cage System (Various PNs) is MAX.

相關臨床試驗

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其他以 Acuity Surgical Devices, LLC 為申請人之記錄

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相關器械(代碼:MAX)

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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