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FDA 510(k)

Thunderbolt™ 低侵入性與Lancer™ 開放椎板螺釘系統

K 號:K171456 · 2017-08-03

申請人Choicespine
決定日期2017-08-03
產品代碼NKB
諮詢委員會或
決定相當於

器材摘要

Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems is the device name listed in this FDA 510(k) record. The listed applicant is Choicespine. It received FDA 510(k) clearance on 2017-08-03 under 510(k) number K171456. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?

Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems is a medical device that received FDA 510(k) clearance on 2017-08-03. The listed applicant is Choicespine. The 510(k) number is K171456.

When did Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems receive FDA 510(k) clearance?

Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems received FDA 510(k) clearance on 2017-08-03, under 510(k) number K171456.

Who is the listed applicant for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?

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

What is the FDA product code for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems?

The FDA product code for Thunderbolt™ Minimally Invasive and Lancer™ Open Pedicle Screw Systems is NKB.

相關臨床試驗

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其他以 Choicespine 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:NKB)

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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