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FDA 510(k)

Dyna Locking Trochanteric Nail™

K 號：K221084 · 2023-03-03

申請人Innosys
決定日期2023-03-03
產品代碼HSB
諮詢委員會或
決定相當於

器材摘要

Dyna Locking Trochanteric Nail™ is the device name listed in this FDA 510(k) record. The listed applicant is Innosys. It received FDA 510(k) clearance on 2023-03-03 under 510(k) number K221084. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dyna Locking Trochanteric Nail™?

Dyna Locking Trochanteric Nail™ is a medical device that received FDA 510(k) clearance on 2023-03-03. The listed applicant is Innosys. The 510(k) number is K221084.

When did Dyna Locking Trochanteric Nail™ receive FDA 510(k) clearance?

Dyna Locking Trochanteric Nail™ received FDA 510(k) clearance on 2023-03-03, under 510(k) number K221084.

Who is the listed applicant for Dyna Locking Trochanteric Nail™?

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

What is the FDA product code for Dyna Locking Trochanteric Nail™?

The FDA product code for Dyna Locking Trochanteric Nail™ is HSB.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

相關器械（代碼：HSB）

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。

K261345兒童釘針平台 髋骨OrthoPediatrics Corp.K261481Pangea 髋骨重建系統Stryker GmbHK253080AND 医療股骨釘系統 (PFNA01); AND 医療股骨釘系統 (PFNA02)Suzhou and Science & Technology Development Corp.K261651Precice™ Max 系統及 Precice™ 腳踝挽救系統NuVasive Specialized OrthopedicsK253155富麗金屬可鎖定內骨髓釘系統Beijing Fule Science & Technology Development Co., Ltd.K253046HERA 開合式硬脊釘系統ZheJiang Decans Medical Devices Co., Ltd.

官方來源

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