FDA 510(k)

NovoGro

K 號：K162087 · 2017-04-18

決定日期2017-04-18

產品代碼MQV

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決定相當於

器材摘要

NovoGro is the device name listed in this FDA 510(k) record. The listed applicant is Osteonovus, Inc.. It received FDA 510(k) clearance on 2017-04-18 under 510(k) number K162087. 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 NovoGro?

NovoGro is a medical device that received FDA 510(k) clearance on 2017-04-18. The listed applicant is Osteonovus, Inc.. The 510(k) number is K162087.

When did NovoGro receive FDA 510(k) clearance?

NovoGro received FDA 510(k) clearance on 2017-04-18, under 510(k) number K162087.

Who is the listed applicant for NovoGro?

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

What is the FDA product code for NovoGro?

The FDA product code for NovoGro is MQV.

其他以 Osteonovus, Inc. 為申請人之記錄

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K173525NovoGro

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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