FDA 510(k)

骨釘直徑 5.0 毫米

K 號：K210717 · 2021-07-12

決定日期2021-07-12

產品代碼PHX

諮詢委員會或

決定相當於

器材摘要

Bone Screws dia. 5,0 mm is the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2021-07-12 under 510(k) number K210717. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Bone Screws dia. 5,0 mm?

Bone Screws dia. 5,0 mm is a medical device that received FDA 510(k) clearance on 2021-07-12. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K210717.

When did Bone Screws dia. 5,0 mm receive FDA 510(k) clearance?

Bone Screws dia. 5,0 mm received FDA 510(k) clearance on 2021-07-12, under 510(k) number K210717.

Who is the listed applicant for Bone Screws dia. 5,0 mm?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bone Screws dia. 5,0 mm?

The FDA product code for Bone Screws dia. 5,0 mm is PHX.

其他以 Lima Corporate S.P.A. 為申請人之記錄

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相關器械（代碼：PHX）

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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