聖托里尼胸椎切除金屬網架系統，卡普里胸椎切除金屬網架系統
K 號：K180665 · 2018-11-28
廣告
器材摘要
SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System is the device name listed in this FDA 510(k) record. The listed applicant is K2m, LLC. It received FDA 510(k) clearance on 2018-11-28 under 510(k) number K180665. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System?
SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System is a medical device that received FDA 510(k) clearance on 2018-11-28. The listed applicant is K2m, LLC. The 510(k) number is K180665.
When did SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System receive FDA 510(k) clearance?
SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System received FDA 510(k) clearance on 2018-11-28, under 510(k) number K180665.
Who is the listed applicant for SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System?
The FDA 510(k) record lists K2m, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System?
The FDA product code for SANTORINI Corpectomy Cage System, CAPRI Corpectomy Cage System is MQP.
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：MQP）
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
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。
廣告