XBraid TT Suture Tape
K 號：K162310 · 2016-11-10
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器材摘要
XBraid TT Suture Tape is the device name listed in this FDA 510(k) record. The listed applicant is Stryker. It received FDA 510(k) clearance on 2016-11-10 under 510(k) number K162310. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the XBraid TT Suture Tape?
XBraid TT Suture Tape is a medical device that received FDA 510(k) clearance on 2016-11-10. The listed applicant is Stryker. The 510(k) number is K162310.
When did XBraid TT Suture Tape receive FDA 510(k) clearance?
XBraid TT Suture Tape received FDA 510(k) clearance on 2016-11-10, under 510(k) number K162310.
Who is the listed applicant for XBraid TT Suture Tape?
The FDA 510(k) record lists Stryker as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XBraid TT Suture Tape?
The FDA product code for XBraid TT Suture Tape is GAT.
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其他以 Stryker 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。
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相關器械（代碼：GAT）
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。
K253910Stitch - Suture Wires and TapesGM Dos Reis Industria e Comercio Ltda.K261021EasyWhip FamilyWinter Innovations, Inc.K260775Polyethylene;Polyethylene Fusion;Polyethylene OrthoTape™Teleflex Medical, LLCK254275HyperSuture All Green Extension LineThreadstone, LLCK254188Meniscus VersaflexGM Dos Reis Industria e Comercio Ltda.K253145Pre-Sutured TendonRti Surgical, 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。
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