FDA 510(k)

Syntec 非无菌史坦曼釘系統

K 號：K200933 · 2020-05-05

決定日期2020-05-05

產品代碼JDW

諮詢委員會或

決定相當於

器材摘要

Syntec Non-Sterile Steinmann Pins System is the device name listed in this FDA 510(k) record. The listed applicant is Syntec Scientific Corporation. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K200933. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Syntec Non-Sterile Steinmann Pins System?

Syntec Non-Sterile Steinmann Pins System is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Syntec Scientific Corporation. The 510(k) number is K200933.

When did Syntec Non-Sterile Steinmann Pins System receive FDA 510(k) clearance?

Syntec Non-Sterile Steinmann Pins System received FDA 510(k) clearance on 2020-05-05, under 510(k) number K200933.

Who is the listed applicant for Syntec Non-Sterile Steinmann Pins System?

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

What is the FDA product code for Syntec Non-Sterile Steinmann Pins System?

The FDA product code for Syntec Non-Sterile Steinmann Pins System is JDW.

其他以 Syntec Scientific Corporation 為申請人之記錄

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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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