膠膜螺釘及膠膜釘釘
K 號：K201561 · 2020-10-05
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器材摘要
Membrane Screws and Membrane Tacks is the device name listed in this FDA 510(k) record. The listed applicant is Neoss Limited. It received FDA 510(k) clearance on 2020-10-05 under 510(k) number K201561. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Membrane Screws and Membrane Tacks?
Membrane Screws and Membrane Tacks is a medical device that received FDA 510(k) clearance on 2020-10-05. The listed applicant is Neoss Limited. The 510(k) number is K201561.
When did Membrane Screws and Membrane Tacks receive FDA 510(k) clearance?
Membrane Screws and Membrane Tacks received FDA 510(k) clearance on 2020-10-05, under 510(k) number K201561.
Who is the listed applicant for Membrane Screws and Membrane Tacks?
The FDA 510(k) record lists Neoss Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Membrane Screws and Membrane Tacks?
The FDA product code for Membrane Screws and Membrane Tacks is DZL.
相關臨床試驗
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相關器械（代碼：DZL）
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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