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FDA 510(k)

梅杜莎-PL籠

K 號：K223654 · 2022-12-28

申請人Medyssey USA, Inc.
決定日期2022-12-28
產品代碼MAX
諮詢委員會或
決定相當於

器材摘要

Medussa-PL Cage is the device name listed in this FDA 510(k) record. The listed applicant is Medyssey USA, Inc.. It received FDA 510(k) clearance on 2022-12-28 under 510(k) number K223654. 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 Medussa-PL Cage?

Medussa-PL Cage is a medical device that received FDA 510(k) clearance on 2022-12-28. The listed applicant is Medyssey USA, Inc.. The 510(k) number is K223654.

When did Medussa-PL Cage receive FDA 510(k) clearance?

Medussa-PL Cage received FDA 510(k) clearance on 2022-12-28, under 510(k) number K223654.

Who is the listed applicant for Medussa-PL Cage?

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

What is the FDA product code for Medussa-PL Cage?

The FDA product code for Medussa-PL Cage is MAX.

相關臨床試驗

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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其他以 Medyssey USA, 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。

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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。

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官方來源

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