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FDA 510(k)

SMR肩關節系統；PRIMA關節盂系統；PRIMA肱骨系統

K 號：K252352 · 2026-01-22

申請人Lima Corporate S.P.A.
決定日期2026-01-22
產品代碼PHX
諮詢委員會或
決定相當於

器材摘要

SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System is the device name listed in this FDA 510(k) record. The listed applicant is Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2026-01-22 under 510(k) number K252352. 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 SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System?

SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K252352.

When did SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System receive FDA 510(k) clearance?

SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System received FDA 510(k) clearance on 2026-01-22, under 510(k) number K252352.

Who is the listed applicant for SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System?

The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System?

The FDA product code for SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral 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 Lima Corporate S.P.A. 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。

K251718ArTT 增強與支撐及骨釘K243826SMR逆向高壓肩關節系統K250980Physica 系統（Physica CR 多孔股骨组件）K243615物理多孔股骨组件K234011AMF TT ConesK233712PRIMA 肱骨系統；PRIMA TT 閃輪

查看所有 41 項裝置 →

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.K260102Tornier Perform Reversed Glenoid和Tornier Perform Reversed Augmented Glenoid Shoulder System的設備名稱Stryker Corporation (Tornier, 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 Orthopedics

官方來源

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