FDA 510(k)

LxHA PEEK 横向內固定系統

K 號：K190684 · 2019-06-17

決定日期2019-06-17

產品代碼MAX

諮詢委員會或

決定相當於

器材摘要

LxHA PEEK Lateral IBF System is the device name listed in this FDA 510(k) record. The listed applicant is Innovasis, Inc.. It received FDA 510(k) clearance on 2019-06-17 under 510(k) number K190684. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LxHA PEEK Lateral IBF System?

LxHA PEEK Lateral IBF System is a medical device that received FDA 510(k) clearance on 2019-06-17. The listed applicant is Innovasis, Inc.. The 510(k) number is K190684.

When did LxHA PEEK Lateral IBF System receive FDA 510(k) clearance?

LxHA PEEK Lateral IBF System received FDA 510(k) clearance on 2019-06-17, under 510(k) number K190684.

Who is the listed applicant for LxHA PEEK Lateral IBF System?

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

What is the FDA product code for LxHA PEEK Lateral IBF System?

The FDA product code for LxHA PEEK Lateral IBF System is MAX.

其他以 Innovasis, Inc. 為申請人之記錄

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相關器械（代碼：MAX）

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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