NuVasive CoRoent Small Ti-C System
K 號：K162138 · 2016-10-26
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器材摘要
NuVasive CoRoent Small Ti-C System is the device name listed in this FDA 510(k) record. The listed applicant is Nu Vasive, Incorporated. It received FDA 510(k) clearance on 2016-10-26 under 510(k) number K162138. 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 NuVasive CoRoent Small Ti-C System?
NuVasive CoRoent Small Ti-C System is a medical device that received FDA 510(k) clearance on 2016-10-26. The listed applicant is Nu Vasive, Incorporated. The 510(k) number is K162138.
When did NuVasive CoRoent Small Ti-C System receive FDA 510(k) clearance?
NuVasive CoRoent Small Ti-C System received FDA 510(k) clearance on 2016-10-26, under 510(k) number K162138.
Who is the listed applicant for NuVasive CoRoent Small Ti-C System?
The FDA 510(k) record lists Nu Vasive, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NuVasive CoRoent Small Ti-C System?
The FDA product code for NuVasive CoRoent Small Ti-C System is ODP.
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其他以 Nu Vasive, Incorporated 為申請人之記錄
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K231735NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasive CoRoent Small Interlock System; NuVasive CoRoent Small Interlock II System; NuVasive CoRoent Small Ti-C System; NuVasive Cohere Cervical Interbody SystemK230894NuVasive Modulus ALIF SystemK230989Rod Registration FrameK223181NuVasive Reline SystemK221751NuVasive Cohere ALIF System Intervertebral Body Fusion DeviceK221388NuVasive Reline Cervical System
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
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