FDA 510(k)

NexGen 独立式前方頸椎間盤切除及融合術（ACDF）系統

K 號：K203129 · 2021-01-12

決定日期2021-01-12

產品代碼OVE

諮詢委員會或

決定相當於

器材摘要

NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System is the device name listed in this FDA 510(k) record. The listed applicant is Precision Spine, Inc.. It received FDA 510(k) clearance on 2021-01-12 under 510(k) number K203129. The device is classified under product code OVE. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System?

NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System is a medical device that received FDA 510(k) clearance on 2021-01-12. The listed applicant is Precision Spine, Inc.. The 510(k) number is K203129.

When did NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System receive FDA 510(k) clearance?

NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System received FDA 510(k) clearance on 2021-01-12, under 510(k) number K203129.

Who is the listed applicant for NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System?

The FDA 510(k) record lists Precision Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System?

The FDA product code for NexGen Standalone Anterior Cervical Discectomy and Fusion (ACDF) System is OVE.

其他以 Precision Spine, Inc. 為申請人之記錄

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。

K250769達科塔LP系統 K242297改革椎板螺釘系統 K231229S-COMP Reform® 即時POCT導航儀器 K220862E-GPS導航儀器 K213118達科塔ALIF系統 K220324AccuFit Lateral 2-Hole Plate

查看所有 17 項裝置 →

相關器械（代碼：OVE）

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。

K263049SABER-C 系統Elevation Spine K261882Pisces-SC 独立颈椎間盤系統Osseus Fusions Systems, LLC K261451ZSAlign脊椎間盤系統ZSFab, Inc.K262094E3D™-C 間體系統Evolution Spine K261279DeltaNEC 間隙系統Nexus Spine K252982CONDUIT™ 零-P™ 維護隔離系統Avalign Technologies, Inc.

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。