FDA 510(k)

正骨科分析軟體

K 號：K183695 · 2019-09-12

決定日期2019-09-12

產品代碼PNN

諮詢委員會DE

決定相當於

器材摘要

OrthoAnalysis Software is the device name listed in this FDA 510(k) record. The listed applicant is Inteware Co., Ltd.. It received FDA 510(k) clearance on 2019-09-12 under 510(k) number K183695. The device is classified under product code PNN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the OrthoAnalysis Software?

OrthoAnalysis Software is a medical device that received FDA 510(k) clearance on 2019-09-12. The listed applicant is Inteware Co., Ltd.. The 510(k) number is K183695.

When did OrthoAnalysis Software receive FDA 510(k) clearance?

OrthoAnalysis Software received FDA 510(k) clearance on 2019-09-12, under 510(k) number K183695.

Who is the listed applicant for OrthoAnalysis Software?

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

What is the FDA product code for OrthoAnalysis Software?

The FDA product code for OrthoAnalysis Software is PNN.

其他以 Inteware Co., Ltd. 為申請人之記錄

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K173965植入計劃軟體

相關器械（代碼：PNN）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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