Trilor 盤片、塊和拱形物
K 號：K173643 · 2018-02-24
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器材摘要
Trilor Disks, Blocks and Arches is the device name listed in this FDA 510(k) record. The listed applicant is Bioloren S.R.L.. It received FDA 510(k) clearance on 2018-02-24 under 510(k) number K173643. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Trilor Disks, Blocks and Arches?
Trilor Disks, Blocks and Arches is a medical device that received FDA 510(k) clearance on 2018-02-24. The listed applicant is Bioloren S.R.L.. The 510(k) number is K173643.
When did Trilor Disks, Blocks and Arches receive FDA 510(k) clearance?
Trilor Disks, Blocks and Arches received FDA 510(k) clearance on 2018-02-24, under 510(k) number K173643.
Who is the listed applicant for Trilor Disks, Blocks and Arches?
The FDA 510(k) record lists Bioloren S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Trilor Disks, Blocks and Arches?
The FDA product code for Trilor Disks, Blocks and Arches is EBF.
相關臨床試驗
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。
相關器械（代碼：EBF）
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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