FAVO S-TLIF
K 號：K190680 · 2019-07-18
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器材摘要
FAVO S-TLIF is the device name listed in this FDA 510(k) record. The listed applicant is Silony Medical GmbH. It received FDA 510(k) clearance on 2019-07-18 under 510(k) number K190680. 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 FAVO S-TLIF?
FAVO S-TLIF is a medical device that received FDA 510(k) clearance on 2019-07-18. The listed applicant is Silony Medical GmbH. The 510(k) number is K190680.
When did FAVO S-TLIF receive FDA 510(k) clearance?
FAVO S-TLIF received FDA 510(k) clearance on 2019-07-18, under 510(k) number K190680.
Who is the listed applicant for FAVO S-TLIF?
The FDA 510(k) record lists Silony Medical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FAVO S-TLIF?
The FDA product code for FAVO S-TLIF is MAX.
其他以 Silony Medical GmbH 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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官方來源
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