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FDA 510(k)

Iatrical 間盤腰椎融合系統（型號 ALIF、型號 TLIF、型號 LLIF）

K 號：K232996 · 2024-09-06

申請人Shanghai Iatrical-Ti Technologies CO , Ltd.
決定日期2024-09-06
產品代碼MAX
諮詢委員會或
決定相當於

器材摘要

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Iatrical-Ti Technologies CO , Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K232996. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Shanghai Iatrical-Ti Technologies CO , Ltd.. The 510(k) number is K232996.

When did Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) receive FDA 510(k) clearance?

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) received FDA 510(k) clearance on 2024-09-06, under 510(k) number K232996.

Who is the listed applicant for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

The FDA 510(k) record lists Shanghai Iatrical-Ti Technologies CO , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF)?

The FDA product code for Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) is MAX.

相關臨床試驗

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相關器械（代碼：MAX）

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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