FDA 510(k)

磁力奧斯柔軟矩陣

K 號：K213959 · 2022-04-14

決定日期2022-04-14

產品代碼MQV

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決定相當於

器材摘要

MagnetOs Flex Matrix is the device name listed in this FDA 510(k) record. The listed applicant is Kuros Biosciences B.V. It received FDA 510(k) clearance on 2022-04-14 under 510(k) number K213959. 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 MagnetOs Flex Matrix?

MagnetOs Flex Matrix is a medical device that received FDA 510(k) clearance on 2022-04-14. The listed applicant is Kuros Biosciences B.V. The 510(k) number is K213959.

When did MagnetOs Flex Matrix receive FDA 510(k) clearance?

MagnetOs Flex Matrix received FDA 510(k) clearance on 2022-04-14, under 510(k) number K213959.

Who is the listed applicant for MagnetOs Flex Matrix?

The FDA 510(k) record lists Kuros Biosciences B.V as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MagnetOs Flex Matrix?

The FDA product code for MagnetOs Flex Matrix is MQV.

其他以 Kuros Biosciences B.V 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。

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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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