FMP擴充型管線
K 號：K172651 · 2017-12-13
廣告
器材摘要
FMP Extended Liners is the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2017-12-13 under 510(k) number K172651. The device is classified under product code OQG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the FMP Extended Liners?
FMP Extended Liners is a medical device that received FDA 510(k) clearance on 2017-12-13. The listed applicant is Encore Medical L.P.. The 510(k) number is K172651.
When did FMP Extended Liners receive FDA 510(k) clearance?
FMP Extended Liners received FDA 510(k) clearance on 2017-12-13, under 510(k) number K172651.
Who is the listed applicant for FMP Extended Liners?
The FDA 510(k) record lists Encore Medical L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FMP Extended Liners?
The FDA product code for FMP Extended Liners is OQG.
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。
其他以 Encore Medical L.P. 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。
相關器械（代碼：OQG）
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。
K202705Prime及DYNASTY® 增材製造殼Microport Orthopedics, Inc.K203472KMTI 髋關節置換系統Kyocera Medical Technologies, Inc.K201660KMTI 髋關節置換系統，Tesera Trabecular Technologies (T3) 骨盂殼系統，多孔骨盂杯系統Kyocera Medical Technologies, Inc.K200328泰莎骨小梁技術公司（T3）骨盂殼系統，多孔骨盂杯系統Kyocera Medical Technologies, Inc.K171543Renovis外科人工髋關節置換系統Renovis Surgical TechnologiesK173104Klassic HD® 折疊式骨盆插管配E-Link® 聚乙烯，Klassic HD® 低矮型骨盆插管配E-Link® 聚乙烯Total Joint Orthopedics, 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。
廣告