福帝連帶TiPlus技術
K 號：K213493 · 2022-01-27
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器材摘要
Fortilink with TiPlus Technology is the device name listed in this FDA 510(k) record. The listed applicant is Paradigm Spine. It received FDA 510(k) clearance on 2022-01-27 under 510(k) number K213493. The device is classified under product code ODP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Fortilink with TiPlus Technology?
Fortilink with TiPlus Technology is a medical device that received FDA 510(k) clearance on 2022-01-27. The listed applicant is Paradigm Spine. The 510(k) number is K213493.
When did Fortilink with TiPlus Technology receive FDA 510(k) clearance?
Fortilink with TiPlus Technology received FDA 510(k) clearance on 2022-01-27, under 510(k) number K213493.
Who is the listed applicant for Fortilink with TiPlus Technology?
The FDA 510(k) record lists Paradigm Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fortilink with TiPlus Technology?
The FDA product code for Fortilink with TiPlus Technology is ODP.
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：ODP）
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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