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FDA 510(k)

MaxBraid 宽頻縫線及 Expressbraid 宽頻移植操作縫線

K 號：K160854 · 2016-12-19

申請人Biomet Manafacturing Corp.
決定日期2016-12-19
產品代碼GAT
諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。
決定相當於

器材摘要

MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manafacturing Corp.. It received FDA 510(k) clearance on 2016-12-19 under 510(k) number K160854. 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 MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture?

MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture is a medical device that received FDA 510(k) clearance on 2016-12-19. The listed applicant is Biomet Manafacturing Corp.. The 510(k) number is K160854.

When did MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture receive FDA 510(k) clearance?

MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture received FDA 510(k) clearance on 2016-12-19, under 510(k) number K160854.

Who is the listed applicant for MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture?

The FDA 510(k) record lists Biomet Manafacturing Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture?

The FDA product code for MaxBraid BroadBand Suture and Expressbraid BroadBand Graft Manipulation Suture is GAT.

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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。

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