FDA 510(k)

ELEOS™ 足保存システムおよびNanoCept® テクノロジー

K番号: K252920 · 2025-10-15

決定日2025-10-15

製品コードQZZ

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

ELEOS™ Limb Salvage System with NanoCept® Technology is the device name listed in this FDA 510(k) record. The listed applicant is Onkos Surgical, Inc.. It received FDA 510(k) clearance on 2025-10-15 under 510(k) number K252920. The device is classified under product code QZZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the ELEOS™ Limb Salvage System with NanoCept® Technology?

ELEOS™ Limb Salvage System with NanoCept® Technology is a medical device that received FDA 510(k) clearance on 2025-10-15. The listed applicant is Onkos Surgical, Inc.. The 510(k) number is K252920.

When did ELEOS™ Limb Salvage System with NanoCept® Technology receive FDA 510(k) clearance?

ELEOS™ Limb Salvage System with NanoCept® Technology received FDA 510(k) clearance on 2025-10-15, under 510(k) number K252920.

Who is the listed applicant for ELEOS™ Limb Salvage System with NanoCept® Technology?

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

What is the FDA product code for ELEOS™ Limb Salvage System with NanoCept® Technology?

The FDA product code for ELEOS™ Limb Salvage System with NanoCept® Technology is QZZ.

申請者としてOnkos Surgical, Inc.を記載するその他の記録

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公式ソース

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