Lucent® XP
K 號：K234150 · 2024-03-27
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器材摘要
Lucent® XP is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Elements. It received FDA 510(k) clearance on 2024-03-27 under 510(k) number K234150. 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 Lucent® XP?
Lucent® XP is a medical device that received FDA 510(k) clearance on 2024-03-27. The listed applicant is Spinal Elements. The 510(k) number is K234150.
When did Lucent® XP receive FDA 510(k) clearance?
Lucent® XP received FDA 510(k) clearance on 2024-03-27, under 510(k) number K234150.
Who is the listed applicant for Lucent® XP?
The FDA 510(k) record lists Spinal Elements as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lucent® XP?
The FDA product code for Lucent® XP is MAX.
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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
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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