FDA 510(k)

ICONN 喬普林干擾螺釘

K 號：K180670 · 2018-12-07

決定日期2018-12-07

產品代碼HWC

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決定相當於

器材摘要

ICONN Campbell Interference Screw is the device name listed in this FDA 510(k) record. The listed applicant is Iconn Orthopedics, LLC. It received FDA 510(k) clearance on 2018-12-07 under 510(k) number K180670. 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 ICONN Campbell Interference Screw?

ICONN Campbell Interference Screw is a medical device that received FDA 510(k) clearance on 2018-12-07. The listed applicant is Iconn Orthopedics, LLC. The 510(k) number is K180670.

When did ICONN Campbell Interference Screw receive FDA 510(k) clearance?

ICONN Campbell Interference Screw received FDA 510(k) clearance on 2018-12-07, under 510(k) number K180670.

Who is the listed applicant for ICONN Campbell Interference Screw?

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

What is the FDA product code for ICONN Campbell Interference Screw?

The FDA product code for ICONN Campbell Interference Screw is HWC. This falls under the Cardiovascular category.

其他以 Iconn Orthopedics, LLC 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：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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