evoDrill 颅骨穿孔器
K 號：K231403 · 2024-03-06
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器材摘要
evoDrill Cranial Perforator is the device name listed in this FDA 510(k) record. The listed applicant is Evonos GmbH & Co. KG. It received FDA 510(k) clearance on 2024-03-06 under 510(k) number K231403. The device is classified under product code HBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the evoDrill Cranial Perforator?
evoDrill Cranial Perforator is a medical device that received FDA 510(k) clearance on 2024-03-06. The listed applicant is Evonos GmbH & Co. KG. The 510(k) number is K231403.
When did evoDrill Cranial Perforator receive FDA 510(k) clearance?
evoDrill Cranial Perforator received FDA 510(k) clearance on 2024-03-06, under 510(k) number K231403.
Who is the listed applicant for evoDrill Cranial Perforator?
The FDA 510(k) record lists Evonos GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for evoDrill Cranial Perforator?
The FDA product code for evoDrill Cranial Perforator is HBF.
相關臨床試驗
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相關器械（代碼：HBF）
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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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