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FDA 510(k)

Montage 可流动 XRO 设定,可吸收止血骨水泥

K号: K231386 · 2023-07-11

决定日期2023-07-11
产品代码MTJ
决定实质等同

器械摘要

Montage Flowable XRO Settable, Resorbable Hemostatic 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 2023-07-11 under 510(k) number K231386. The device is classified under product code MTJ. FDA Decision: Substantially Equivalent.

常见问题

What is the Montage Flowable XRO Settable, Resorbable Hemostatic Bone Paste?

Montage Flowable XRO Settable, Resorbable Hemostatic Bone Paste is a medical device that received FDA 510(k) clearance on 2023-07-11. The listed applicant is Orthocon, Inc.. The 510(k) number is K231386.

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

Montage Flowable XRO Settable, Resorbable Hemostatic Bone Paste received FDA 510(k) clearance on 2023-07-11, under 510(k) number K231386.

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

FDA 510(k)记录中列出Orthocon, Inc.为申请人。这本身并不能确立该设备制造商的身份。

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

The FDA product code for Montage Flowable XRO Settable, Resorbable Hemostatic Bone Paste is MTJ.

相关临床试验

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列明Orthocon, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

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相关器械(代码:MTJ)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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