FDA 510(k)

エチレンオキシド滅菌供給元の変更：MPOヒップ用

K番号: K240046 · 2024-04-18

決定日2024-04-18

製品コードLPH

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

Ethylene Oxide Sterilization Supplier Change for MPO Hips is the device name listed in this FDA 510(k) record. The listed applicant is Microport Orthopedics. It received FDA 510(k) clearance on 2024-04-18 under 510(k) number K240046. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Ethylene Oxide Sterilization Supplier Change for MPO Hips?

Ethylene Oxide Sterilization Supplier Change for MPO Hips is a medical device that received FDA 510(k) clearance on 2024-04-18. The listed applicant is Microport Orthopedics. The 510(k) number is K240046.

When did Ethylene Oxide Sterilization Supplier Change for MPO Hips receive FDA 510(k) clearance?

Ethylene Oxide Sterilization Supplier Change for MPO Hips received FDA 510(k) clearance on 2024-04-18, under 510(k) number K240046.

Who is the listed applicant for Ethylene Oxide Sterilization Supplier Change for MPO Hips?

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

What is the FDA product code for Ethylene Oxide Sterilization Supplier Change for MPO Hips?

The FDA product code for Ethylene Oxide Sterilization Supplier Change for MPO Hips is LPH.

公式ソース

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エチレンオキシド滅菌供給元の変更：MPOヒップ用

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：LPH）

公式ソース