FDA 510(k)

TrellOss™-L MPF

K 號：K192687 · 2020-01-09

決定日期2020-01-09

產品代碼MAX

諮詢委員會或

決定相當於

器材摘要

TrellOss™-L MPF is the device name listed in this FDA 510(k) record. The listed applicant is Nexxt Spine, LLC. It received FDA 510(k) clearance on 2020-01-09 under 510(k) number K192687. 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 TrellOss™-L MPF?

TrellOss™-L MPF is a medical device that received FDA 510(k) clearance on 2020-01-09. The listed applicant is Nexxt Spine, LLC. The 510(k) number is K192687.

When did TrellOss™-L MPF receive FDA 510(k) clearance?

TrellOss™-L MPF received FDA 510(k) clearance on 2020-01-09, under 510(k) number K192687.

Who is the listed applicant for TrellOss™-L MPF?

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

What is the FDA product code for TrellOss™-L MPF?

The FDA product code for TrellOss™-L MPF is MAX.

其他以 Nexxt Spine, LLC 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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