FDA 510(k)

AOS小骨釘システム

K番号: K163014 · 2017-01-24

申請者Advanced Orthopaedic Solutions, Inc. (Aos)

決定日2017-01-24

製品コードHSB

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

AOS Small Bone Nailing System is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Orthopaedic Solutions, Inc. (Aos). It received FDA 510(k) clearance on 2017-01-24 under 510(k) number K163014. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the AOS Small Bone Nailing System?

AOS Small Bone Nailing System is a medical device that received FDA 510(k) clearance on 2017-01-24. The listed applicant is Advanced Orthopaedic Solutions, Inc. (Aos). The 510(k) number is K163014.

When did AOS Small Bone Nailing System receive FDA 510(k) clearance?

AOS Small Bone Nailing System received FDA 510(k) clearance on 2017-01-24, under 510(k) number K163014.

Who is the listed applicant for AOS Small Bone Nailing System?

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

What is the FDA product code for AOS Small Bone Nailing System?

The FDA product code for AOS Small Bone Nailing System is HSB.

申請者としてAdvanced Orthopaedic Solutions, Inc. (Aos)を記載するその他の記録

K181035AOS小骨折プレートシステムライト K171606AOS前外側近位上腕骨プレート K161913AOS小骨折プレートシステム

公式ソース

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