FDA 510(k)

泰魯斯後枕顱頸胸脊椎系統

K 號：K253195 · 2026-06-02

申請人ZheJiang Decans Medical Devices Co., Ltd.

決定日期2026-06-02

產品代碼NKG

諮詢委員會或

決定相當於

器材摘要

TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems is the device name listed in this FDA 510(k) record. The listed applicant is ZheJiang Decans Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K253195. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems?

TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is ZheJiang Decans Medical Devices Co., Ltd.. The 510(k) number is K253195.

When did TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems receive FDA 510(k) clearance?

TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems received FDA 510(k) clearance on 2026-06-02, under 510(k) number K253195.

Who is the listed applicant for TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems?

The FDA 510(k) record lists ZheJiang Decans Medical Devices Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems?

The FDA product code for TAURUS Posterior Occipital-Cervico-Thoracic Spinal Systems is NKG.

其他以 ZheJiang Decans Medical Devices Co., Ltd. 為申請人之記錄

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相關器械（代碼：NKG）

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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