FDA 510(k)

Vitoss BiModal Bone Graft Substitute Foam Strip

K番号: K153608 · 2016-02-12

決定日2016-02-12

製品コードMQV

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OR [翻訳] OR 注：原文が具体的な内容を含んでいないため、翻訳は単なる「OR」のままです。

決定大幅同等

医療機器の概要

Vitoss BiModal Bone Graft Substitute Foam Strip is the device name listed in this FDA 510(k) record. The listed applicant is Orthovita, Inc.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K153608. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Vitoss BiModal Bone Graft Substitute Foam Strip?

Vitoss BiModal Bone Graft Substitute Foam Strip is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Orthovita, Inc.. The 510(k) number is K153608.

When did Vitoss BiModal Bone Graft Substitute Foam Strip receive FDA 510(k) clearance?

Vitoss BiModal Bone Graft Substitute Foam Strip received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153608.

Who is the listed applicant for Vitoss BiModal Bone Graft Substitute Foam Strip?

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

What is the FDA product code for Vitoss BiModal Bone Graft Substitute Foam Strip?

The FDA product code for Vitoss BiModal Bone Graft Substitute Foam Strip is MQV.

申請者としてOrthovita, Inc.を記載するその他の記録

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