FDA 510(k)

NuVasive AttraX 床架

K 號：K240507 · 2024-03-20

決定日期2024-03-20

產品代碼MQV

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器材摘要

NuVasive AttraX Scaffold is the device name listed in this FDA 510(k) record. The listed applicant is Nuvasive, Inc.. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K240507. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NuVasive AttraX Scaffold?

NuVasive AttraX Scaffold is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Nuvasive, Inc.. The 510(k) number is K240507.

When did NuVasive AttraX Scaffold receive FDA 510(k) clearance?

NuVasive AttraX Scaffold received FDA 510(k) clearance on 2024-03-20, under 510(k) number K240507.

Who is the listed applicant for NuVasive AttraX Scaffold?

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

What is the FDA product code for NuVasive AttraX Scaffold?

The FDA product code for NuVasive AttraX Scaffold is MQV.

其他以 Nuvasive, Inc. 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。

K223731NuVasive Modulus-C 間體系統 K211757簡化監控器 K173117NuVasive® VersaTie™ 系統

相關器械（代碼：MQV）

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。

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