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FDA 510(k)

TruLift® 横向擴展式間隔與横向支撐板系統

K 號:K251502 · 2025-07-07

決定日期2025-07-07
產品代碼MAX
諮詢委員會或
決定相當於

器材摘要

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine, Inc.. It received FDA 510(k) clearance on 2025-07-07 under 510(k) number K251502. 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 TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is a medical device that received FDA 510(k) clearance on 2025-07-07. The listed applicant is Life Spine, Inc.. The 510(k) number is K251502.

When did TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System receive FDA 510(k) clearance?

TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System received FDA 510(k) clearance on 2025-07-07, under 510(k) number K251502.

Who is the listed applicant for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

FDA 510(k) 記錄將 Life Spine, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System?

The FDA product code for TruLift® Lateral Expandable Spacer & Lateral Buttress Plate System is MAX.

相關臨床試驗

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其他以 Life Spine, Inc. 為申請人之記錄

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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。

官方來源

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