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FDA 510(k)

Stablyx CMC關節置换植入系統

K 號:K180744 · 2018-04-11

決定日期2018-04-11
產品代碼KYI
諮詢委員會或
決定相當於

器材摘要

Stablyx CMC Arthroplasty Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Skeletal Dynamics, LLC. It received FDA 510(k) clearance on 2018-04-11 under 510(k) number K180744. The device is classified under product code KYI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Stablyx CMC Arthroplasty Implant System?

Stablyx CMC Arthroplasty Implant System is a medical device that received FDA 510(k) clearance on 2018-04-11. The listed applicant is Skeletal Dynamics, LLC. The 510(k) number is K180744.

When did Stablyx CMC Arthroplasty Implant System receive FDA 510(k) clearance?

Stablyx CMC Arthroplasty Implant System received FDA 510(k) clearance on 2018-04-11, under 510(k) number K180744.

Who is the listed applicant for Stablyx CMC Arthroplasty Implant System?

The FDA 510(k) record lists Skeletal Dynamics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Stablyx CMC Arthroplasty Implant System?

The FDA product code for Stablyx CMC Arthroplasty Implant System is KYI.

相關臨床試驗

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。

其他以 Skeletal Dynamics, LLC 為申請人之記錄

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。

相關器械(代碼:KYI)

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。

官方來源

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