FDA 510(k)

MotoBAND CP 嵌入式系統

K 號：K173710 · 2018-02-12

決定日期2018-02-12

產品代碼HWC

諮詢委員會或

決定相當於

器材摘要

MotoBAND CP Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Crossroads Extremity Systems, LLC. It received FDA 510(k) clearance on 2018-02-12 under 510(k) number K173710. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the MotoBAND CP Implant System?

MotoBAND CP Implant System is a medical device that received FDA 510(k) clearance on 2018-02-12. The listed applicant is Crossroads Extremity Systems, LLC. The 510(k) number is K173710.

When did MotoBAND CP Implant System receive FDA 510(k) clearance?

MotoBAND CP Implant System received FDA 510(k) clearance on 2018-02-12, under 510(k) number K173710.

Who is the listed applicant for MotoBAND CP Implant System?

The FDA 510(k) record lists Crossroads Extremity Systems, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MotoBAND CP Implant System?

The FDA product code for MotoBAND CP Implant System is HWC. This falls under the Cardiovascular category.

其他以 Crossroads Extremity Systems, LLC 為申請人之記錄

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相關器械（代碼：HWC）

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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