FDA 510(k)

量子® 全踝人工關節

K 號：K191380 · 2020-01-29

決定日期2020-01-29

產品代碼HSN

諮詢委員會或

決定相當於

器材摘要

Quantum® Total Ankle Prosthesis is the device name listed in this FDA 510(k) record. The listed applicant is In2bones Sas. It received FDA 510(k) clearance on 2020-01-29 under 510(k) number K191380. The device is classified under product code HSN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Quantum® Total Ankle Prosthesis?

Quantum® Total Ankle Prosthesis is a medical device that received FDA 510(k) clearance on 2020-01-29. The listed applicant is In2bones Sas. The 510(k) number is K191380.

When did Quantum® Total Ankle Prosthesis receive FDA 510(k) clearance?

Quantum® Total Ankle Prosthesis received FDA 510(k) clearance on 2020-01-29, under 510(k) number K191380.

Who is the listed applicant for Quantum® Total Ankle Prosthesis?

The FDA 510(k) record lists In2bones Sas as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Quantum® Total Ankle Prosthesis?

The FDA product code for Quantum® Total Ankle Prosthesis is HSN.

其他以 In2bones Sas 為申請人之記錄

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相關器械（代碼：HSN）

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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