FDA 510(k)

EffortMed PEEK 金屬網格與椎體切除金屬網格

K 號：K252686 · 2025-11-21

決定日期2025-11-21

產品代碼ODP

諮詢委員會或

決定相當於

器材摘要

EffortMed PEEK Cages & Corpectomy Cages is the device name listed in this FDA 510(k) record. The listed applicant is Effortmed, LLC. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K252686. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EffortMed PEEK Cages & Corpectomy Cages?

EffortMed PEEK Cages & Corpectomy Cages is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Effortmed, LLC. The 510(k) number is K252686.

When did EffortMed PEEK Cages & Corpectomy Cages receive FDA 510(k) clearance?

EffortMed PEEK Cages & Corpectomy Cages received FDA 510(k) clearance on 2025-11-21, under 510(k) number K252686.

Who is the listed applicant for EffortMed PEEK Cages & Corpectomy Cages?

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

What is the FDA product code for EffortMed PEEK Cages & Corpectomy Cages?

The FDA product code for EffortMed PEEK Cages & Corpectomy Cages is ODP.

其他以 Effortmed, LLC 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。

K243946EffortMed脊椎固定系統 K240935ARENAL前颈椎板系统

相關器械（代碼：ODP）

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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