維達康連接TLIF金屬內固定器
K 號：K203327 · 2021-01-25
廣告
器材摘要
VERTACONNECT TLIF Cage is the device name listed in this FDA 510(k) record. The listed applicant is Signus Medizintechnik. It received FDA 510(k) clearance on 2021-01-25 under 510(k) number K203327. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the VERTACONNECT TLIF Cage?
VERTACONNECT TLIF Cage is a medical device that received FDA 510(k) clearance on 2021-01-25. The listed applicant is Signus Medizintechnik. The 510(k) number is K203327.
When did VERTACONNECT TLIF Cage receive FDA 510(k) clearance?
VERTACONNECT TLIF Cage received FDA 510(k) clearance on 2021-01-25, under 510(k) number K203327.
Who is the listed applicant for VERTACONNECT TLIF Cage?
The FDA 510(k) record lists Signus Medizintechnik as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERTACONNECT TLIF Cage?
The FDA product code for VERTACONNECT TLIF Cage is MAX.
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：MAX）
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。
K261049SCALA® TLSpineart SAK261430TruLift可擴展系統Life Spine, Inc.K253011Catalyft PL 可擴展椎間體系統Medtronic Sofamor Danek USA, Inc.K261020Symmetrix™ L脊椎系統Medtronic Sofamor Danek USA, Inc.K253420Admiral ACP System; Explorer TO System; Laminoplasty System; Manta Ray TDF Spacer; Meridian Interbody System; Meridian Anterior Plate System; Reef L Interbody System; Reef TO/TA System; Regatta Lateral System; Regatta Lateral Plate System; Shoreline ACS Interbody System; Shoreline Threaded TruProfile Plate; Shoreline RT Interbody System; Vu Mesh; WaveForm A Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TA Interbody System; WaveForm TO Interbody SystemSeaSpine Orthopedics CorporationK253151Fule間體融合籠架系統Beijing Fule Science & Technology Development Co., Ltd.
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