填充物，骨空洞，合成肽
PMA 核准號：P240001 · 2026-09-16
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器材摘要
Filler, bone void, synthetic peptide is the device name listed in this FDA 510(k) record. The listed applicant is Cerapedics, Inc.. It received FDA 510(k) clearance on 2026-09-16. The device is classified under product code NOX. It was reviewed by the OR advisory panel.
常見問題
What is the Filler, bone void, synthetic peptide?
Filler, bone void, synthetic peptide is a medical device that received FDA 510(k) clearance on 2026-09-16. The listed applicant is Cerapedics, Inc..
When did Filler, bone void, synthetic peptide receive FDA 510(k) clearance?
The clearance date for Filler, bone void, synthetic peptide can be found in the official FDA records.
誰是填充劑、骨空洞、合成肽的登記申請人？
The FDA 510(k) record lists Cerapedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為Filler，骨空洞，合成肽是什麼？
FDA產品代碼，對於填充劑、骨空洞、合成肽為NOX。
相關臨床試驗
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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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