Orbitum骨釘植入體，X和VI
K 號：K173693 · 2018-02-23
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器材摘要
Orbitum Bone Staple Implant, X and VI is the device name listed in this FDA 510(k) record. The listed applicant is Orthovestments, LLC. It received FDA 510(k) clearance on 2018-02-23 under 510(k) number K173693. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Orbitum Bone Staple Implant, X and VI?
Orbitum Bone Staple Implant, X and VI is a medical device that received FDA 510(k) clearance on 2018-02-23. The listed applicant is Orthovestments, LLC. The 510(k) number is K173693.
When did Orbitum Bone Staple Implant, X and VI receive FDA 510(k) clearance?
Orbitum Bone Staple Implant, X and VI received FDA 510(k) clearance on 2018-02-23, under 510(k) number K173693.
Who is the listed applicant for Orbitum Bone Staple Implant, X and VI?
The FDA 510(k) record lists Orthovestments, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Orbitum Bone Staple Implant, X and VI?
The FDA product code for Orbitum Bone Staple Implant, X and VI is JDR.
相關臨床試驗
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相關器械（代碼：JDR）
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
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