FDA 510(k)

人工骨膠

K 號：K240458 · 2024-03-07

決定日期2024-03-07

產品代碼MQV

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決定相當於

器材摘要

Synthetic Bone Putty is the device name listed in this FDA 510(k) record. The listed applicant is Ventris Medical. It received FDA 510(k) clearance on 2024-03-07 under 510(k) number K240458. 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 Synthetic Bone Putty?

Synthetic Bone Putty is a medical device that received FDA 510(k) clearance on 2024-03-07. The listed applicant is Ventris Medical. The 510(k) number is K240458.

When did Synthetic Bone Putty receive FDA 510(k) clearance?

Synthetic Bone Putty received FDA 510(k) clearance on 2024-03-07, under 510(k) number K240458.

Who is the listed applicant for Synthetic Bone Putty?

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

What is the FDA product code for Synthetic Bone Putty?

The FDA product code for Synthetic Bone Putty is MQV.

其他以 Ventris Medical 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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