FDA 510(k)

MOSS VRS脊椎系統

K 號：K203607 · 2021-08-20

決定日期2021-08-20

產品代碼NKB

諮詢委員會或

決定相當於

器材摘要

MOSS VRS Spinal System is the device name listed in this FDA 510(k) record. The listed applicant is Biedermann Motech GmbH & Co. KG. It received FDA 510(k) clearance on 2021-08-20 under 510(k) number K203607. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MOSS VRS Spinal System?

MOSS VRS Spinal System is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Biedermann Motech GmbH & Co. KG. The 510(k) number is K203607.

When did MOSS VRS Spinal System receive FDA 510(k) clearance?

MOSS VRS Spinal System received FDA 510(k) clearance on 2021-08-20, under 510(k) number K203607.

Who is the listed applicant for MOSS VRS Spinal System?

The FDA 510(k) record lists Biedermann Motech GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOSS VRS Spinal System?

The FDA product code for MOSS VRS Spinal System is NKB.

其他以 Biedermann Motech GmbH & Co. KG 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：NKB）

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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