FDA 510(k)

導向成長板系統＋

K 號：K180624 · 2018-05-15

決定日期2018-05-15

產品代碼OBT

諮詢委員會或

決定相當於

器材摘要

Guided Growth Plate System Plus is the device name listed in this FDA 510(k) record. The listed applicant is Orthofix Srl. It received FDA 510(k) clearance on 2018-05-15 under 510(k) number K180624. The device is classified under product code OBT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Guided Growth Plate System Plus?

Guided Growth Plate System Plus is a medical device that received FDA 510(k) clearance on 2018-05-15. The listed applicant is Orthofix Srl. The 510(k) number is K180624.

When did Guided Growth Plate System Plus receive FDA 510(k) clearance?

Guided Growth Plate System Plus received FDA 510(k) clearance on 2018-05-15, under 510(k) number K180624.

Who is the listed applicant for Guided Growth Plate System Plus?

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

What is the FDA product code for Guided Growth Plate System Plus?

The FDA product code for Guided Growth Plate System Plus is OBT.

其他以 Orthofix Srl 為申請人之記錄

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相關器械（代碼：OBT）

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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官方來源

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