Hoffman LRF System
K 號：K161753 · 2016-11-15
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器材摘要
Hoffman LRF System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker GmbH. It received FDA 510(k) clearance on 2016-11-15 under 510(k) number K161753. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Hoffman LRF System?
Hoffman LRF System is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is Stryker GmbH. The 510(k) number is K161753.
When did Hoffman LRF System receive FDA 510(k) clearance?
Hoffman LRF System received FDA 510(k) clearance on 2016-11-15, under 510(k) number K161753.
Who is the listed applicant for Hoffman LRF System?
The FDA 510(k) record lists Stryker GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hoffman LRF System?
The FDA product code for Hoffman LRF System is KTT.
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其他以 Stryker GmbH 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。
K261481Pangea Femur Reconstruction SystemK253640T2 Alpha Femur Retrograde Nailing System; Pangea Femur Reconstruction SystemK253202Hoffmann LRF SystemK251400T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing SystemK250163T2 Alpha股骨遠端釘固定系統K242445Pangea Platform; Pangea Femur Plating System; Pangea Humerus Plating System; Pangea Tibia Plating System
相關器械（代碼：KTT）
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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