Zimmer M/L Taper Hip Prosthesis
K 號：K161830 · 2016-10-26
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器材摘要
Zimmer M/L Taper Hip Prosthesis is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2016-10-26 under 510(k) number K161830. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Zimmer M/L Taper Hip Prosthesis?
Zimmer M/L Taper Hip Prosthesis is a medical device that received FDA 510(k) clearance on 2016-10-26. The listed applicant is Zimmer, Inc.. The 510(k) number is K161830.
When did Zimmer M/L Taper Hip Prosthesis receive FDA 510(k) clearance?
Zimmer M/L Taper Hip Prosthesis received FDA 510(k) clearance on 2016-10-26, under 510(k) number K161830.
Who is the listed applicant for Zimmer M/L Taper Hip Prosthesis?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Zimmer M/L Taper Hip Prosthesis?
The FDA product code for Zimmer M/L Taper Hip Prosthesis is LZO.
相關臨床試驗
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其他以 Zimmer, 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。
K262955OsseoFit Stemless Shoulder SystemK260831Z1 Hip SystemK261683Augment Off-Axis Instrument SystemK251840Zimmer® Persona® Personalized Knee SystemK260182Avenir® Müller Stem; Avenir Complete™ Hip SystemK253592Zimmer Biomet Reverse Shoulder Prosthesis (Alliance Humeral Bearings, Identity Humeral Trays, Comprehensive Reverse Humeral Trays, Comprehensive Reverse 32mm Glenospheres and Adapter)
相關器械（代碼：LZO）
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。
K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH
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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