免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料，僅供一般參考，不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

Tornier Perform Reversed Glenoid和Tornier Perform Reversed Augmented Glenoid Shoulder System的設備名稱

K 號：K260102 · 2026-06-12

申請人Stryker Corporation (Tornier, Inc.)
決定日期2026-06-12
產品代碼PHX
諮詢委員會或
決定相當於

器材摘要

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation (Tornier, Inc.). It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K260102. The device is classified under product code PHX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Stryker Corporation (Tornier, Inc.). The 510(k) number is K260102.

When did Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System receive FDA 510(k) clearance?

Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System received FDA 510(k) clearance on 2026-06-12, under 510(k) number K260102.

Who is the listed applicant for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

The FDA 510(k) record lists Stryker Corporation (Tornier, Inc.) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System?

The FDA product code for Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder System is PHX.

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

其他以 Stryker Corporation (Tornier, Inc.) 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。

K241878Tornier肩胛骨重建系統（Tornier HRS）；Tornier Perform肩胛骨系統 - 植骨（Tornier PHS-Stem）K241609Tornier 肱骨重建系統 (Tornier HRS)

相關器械（代碼：PHX）

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。

K260556Veritas肩部系統Restor3DK261683Augment 偏心儀器系統Zimmer, Inc.K261016MSS - 肱骨反覆蓋擴充件Medacta International, SAK253992Veritas逆向全肩關節系統Restor3DK252404全面反向肩蓋 - HA 髖關節基板Biomet OrthopedicsK260583Equinoxe® 肩關節系統Exactech, Inc.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。

↑