FDA 510(k)

変形分析および矯正ソフトウェア（DACS）および機器

K番号: K180539 · 2018-08-13

申請者Arrowhead Medical Device Technologies, LLC

決定日2018-08-13

製品コードOSN

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

Deformity Analysis and Correction Software (DACS) and Instrumentation is the device name listed in this FDA 510(k) record. The listed applicant is Arrowhead Medical Device Technologies, LLC. It received FDA 510(k) clearance on 2018-08-13 under 510(k) number K180539. The device is classified under product code OSN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Deformity Analysis and Correction Software (DACS) and Instrumentation?

Deformity Analysis and Correction Software (DACS) and Instrumentation is a medical device that received FDA 510(k) clearance on 2018-08-13. The listed applicant is Arrowhead Medical Device Technologies, LLC. The 510(k) number is K180539.

When did Deformity Analysis and Correction Software (DACS) and Instrumentation receive FDA 510(k) clearance?

Deformity Analysis and Correction Software (DACS) and Instrumentation received FDA 510(k) clearance on 2018-08-13, under 510(k) number K180539.

Who is the listed applicant for Deformity Analysis and Correction Software (DACS) and Instrumentation?

The FDA 510(k) record lists Arrowhead Medical Device Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Deformity Analysis and Correction Software (DACS) and Instrumentation?

The FDA product code for Deformity Analysis and Correction Software (DACS) and Instrumentation is OSN.

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変形分析および矯正ソフトウェア（DACS）および機器

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：OSN）

公式ソース