FDA 510(k)

Vector™脊椎螺釘系統

K 號：K241276 · 2024-05-20

決定日期2024-05-20

產品代碼NKB

諮詢委員會或

決定相當於

器材摘要

Vector™ Pedicle Screw System is the device name listed in this FDA 510(k) record. The listed applicant is Innovasis, Inc.. It received FDA 510(k) clearance on 2024-05-20 under 510(k) number K241276. 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 Vector™ Pedicle Screw System?

Vector™ Pedicle Screw System is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Innovasis, Inc.. The 510(k) number is K241276.

When did Vector™ Pedicle Screw System receive FDA 510(k) clearance?

Vector™ Pedicle Screw System received FDA 510(k) clearance on 2024-05-20, under 510(k) number K241276.

Who is the listed applicant for Vector™ Pedicle Screw System?

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

What is the FDA product code for Vector™ Pedicle Screw System?

The FDA product code for Vector™ Pedicle Screw System is NKB.

其他以 Innovasis, Inc. 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。

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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。

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官方來源

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