iNSitu 外側骨盆內襯,iNSitu 髋臥骨柄帶等离子體噴射CPTi塗層
K 號:K243192 · 2026-06-05
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器材摘要
常見問題
What is the iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating?
iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating is a medical device that received FDA 510(k) clearance on 2026-06-05. The listed applicant is Nextstep Arthopedix, LLC. The 510(k) number is K243192.
When did iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating receive FDA 510(k) clearance?
iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating received FDA 510(k) clearance on 2026-06-05, under 510(k) number K243192.
Who is the listed applicant for iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating?
The FDA 510(k) record lists Nextstep Arthopedix, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating?
The FDA product code for iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi Coating is LPH.
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。
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。
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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