NGM 波浪 PLIF 金屬架
K 號：K212050 · 2021-12-01
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器材摘要
NGM WAVE PLIF Cage is the device name listed in this FDA 510(k) record. The listed applicant is NGMedical GmbH. It received FDA 510(k) clearance on 2021-12-01 under 510(k) number K212050. 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 NGM WAVE PLIF Cage?
NGM WAVE PLIF Cage is a medical device that received FDA 510(k) clearance on 2021-12-01. The listed applicant is NGMedical GmbH. The 510(k) number is K212050.
When did NGM WAVE PLIF Cage receive FDA 510(k) clearance?
NGM WAVE PLIF Cage received FDA 510(k) clearance on 2021-12-01, under 510(k) number K212050.
Who is the listed applicant for NGM WAVE PLIF Cage?
The FDA 510(k) record lists NGMedical GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NGM WAVE PLIF Cage?
The FDA product code for NGM WAVE PLIF Cage is MAX.
其他以 NGMedical 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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