FDA 510(k)

蒙特奇流動可調骨膠膠泥

K 號：K231270 · 2023-09-01

決定日期2023-09-01

產品代碼MQV

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決定相當於

器材摘要

Montage Flowable Settable, Resorbable Bone Paste is the device name listed in this FDA 510(k) record. The listed applicant is Orthocon, Inc.. It received FDA 510(k) clearance on 2023-09-01 under 510(k) number K231270. 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 Montage Flowable Settable, Resorbable Bone Paste?

Montage Flowable Settable, Resorbable Bone Paste is a medical device that received FDA 510(k) clearance on 2023-09-01. The listed applicant is Orthocon, Inc.. The 510(k) number is K231270.

When did Montage Flowable Settable, Resorbable Bone Paste receive FDA 510(k) clearance?

Montage Flowable Settable, Resorbable Bone Paste received FDA 510(k) clearance on 2023-09-01, under 510(k) number K231270.

Who is the listed applicant for Montage Flowable Settable, Resorbable Bone Paste?

FDA 510(k) 記錄將 Orthocon, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Montage Flowable Settable, Resorbable Bone Paste?

The FDA product code for Montage Flowable Settable, Resorbable Bone Paste is MQV.

其他以 Orthocon, 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：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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官方來源

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