FDA 510(k)

無情脊柱RJB

K 號：K252615 · 2025-09-17

決定日期2025-09-17

產品代碼QWL

諮詢委員會或

決定相當於

器材摘要

Ruthless Spine RJB is the device name listed in this FDA 510(k) record. The listed applicant is Ruthless, LLC Dba Ruthless Spine. It received FDA 510(k) clearance on 2025-09-17 under 510(k) number K252615. The device is classified under product code QWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ruthless Spine RJB?

Ruthless Spine RJB is a medical device that received FDA 510(k) clearance on 2025-09-17. The listed applicant is Ruthless, LLC Dba Ruthless Spine. The 510(k) number is K252615.

When did Ruthless Spine RJB receive FDA 510(k) clearance?

Ruthless Spine RJB received FDA 510(k) clearance on 2025-09-17, under 510(k) number K252615.

Who is the listed applicant for Ruthless Spine RJB?

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

What is the FDA product code for Ruthless Spine RJB?

The FDA product code for Ruthless Spine RJB is QWL.

其他以 Ruthless, LLC Dba Ruthless Spine 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。

K243375無情脊柱RJB

相關器械（代碼：QWL）

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。

K243375無情脊柱RJBRuthless, LLC Dba Ruthless Spine

官方來源

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