Latitud™ 髋關節置換系統
K 號：K222436 · 2023-05-09
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器材摘要
Latitud™ Hip Replacement System is the device name listed in this FDA 510(k) record. The listed applicant is Meril Healthcare Pvt. , Ltd.. It received FDA 510(k) clearance on 2023-05-09 under 510(k) number K222436. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Latitud™ Hip Replacement System?
Latitud™ Hip Replacement System is a medical device that received FDA 510(k) clearance on 2023-05-09. The listed applicant is Meril Healthcare Pvt. , Ltd.. The 510(k) number is K222436.
When did Latitud™ Hip Replacement System receive FDA 510(k) clearance?
Latitud™ Hip Replacement System received FDA 510(k) clearance on 2023-05-09, under 510(k) number K222436.
Who is the listed applicant for Latitud™ Hip Replacement System?
The FDA 510(k) record lists Meril Healthcare Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Latitud™ Hip Replacement System?
The FDA product code for Latitud™ Hip Replacement System is LPH.
相關臨床試驗
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其他以 Meril Healthcare Pvt. , Ltd. 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。
K222816豪華TiNbN塗層膝關節K212839豪華TiNbN塗層膝關節K183532Latitud 髋關節置換系統K172857Latitud 髋關節置換系統K171320ARMAR / ARTIS 小骨碎片和跟骨板 & MBOSS / FIXION 螺丝, ARMAR/ ARTIS 肱骨和桡骨远端板 & MBOSS/FIXION 螺丝, ARMAR / ARTIS 胫骨和支撑板 & MBOSS/FIXION 螺丝, ARMAR / ARTIS 2.4mm 板 & MBOSS/FIXION 螺丝, ARMAR/ ARTIS 锁骨钩板 & MBOSS/FIXION 螺丝, ARMAR/ ARTIS 干骺端板 & MBOSS/FIXION 螺丝, ARMAR / ARTIS 跟骨板 & MBOSS/FIXION 螺丝K172936Destiknee™ 全膝系統
相關器械（代碼：LPH）
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
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。
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