FDA 510(k)

可塑骨空洞填充物及可塑骨空洞填充物 + CCC

K 號：K241555 · 2025-02-21

決定日期2025-02-21

產品代碼MQV

諮詢委員會或

決定相當於

器材摘要

Moldable Bone Void Filler and Moldable Bone Void Filler + CCC is the device name listed in this FDA 510(k) record. The listed applicant is Rti Surgical, Inc.. It received FDA 510(k) clearance on 2025-02-21 under 510(k) number K241555. 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 Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?

Moldable Bone Void Filler and Moldable Bone Void Filler + CCC is a medical device that received FDA 510(k) clearance on 2025-02-21. The listed applicant is Rti Surgical, Inc.. The 510(k) number is K241555.

When did Moldable Bone Void Filler and Moldable Bone Void Filler + CCC receive FDA 510(k) clearance?

Moldable Bone Void Filler and Moldable Bone Void Filler + CCC received FDA 510(k) clearance on 2025-02-21, under 510(k) number K241555.

Who is the listed applicant for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?

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

What is the FDA product code for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC?

The FDA product code for Moldable Bone Void Filler and Moldable Bone Void Filler + CCC is MQV.

其他以 Rti Surgical, Inc. 為申請人之記錄

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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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