Cube 导航器
K号: K240620 · 2024-03-25
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器械摘要
Cube Navigator is the device name listed in this FDA 510(k) record. The listed applicant is Medical Templates AG. It received FDA 510(k) clearance on 2024-03-25 under 510(k) number K240620. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cube Navigator?
Cube Navigator is a medical device that received FDA 510(k) clearance on 2024-03-25. The listed applicant is Medical Templates AG. The 510(k) number is K240620.
When did Cube Navigator receive FDA 510(k) clearance?
Cube Navigator received FDA 510(k) clearance on 2024-03-25, under 510(k) number K240620.
Who is the listed applicant for Cube Navigator?
The FDA 510(k) record lists Medical Templates AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cube Navigator?
The FDA product code for Cube Navigator is LLZ.
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相关器械（代码：LLZ）
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请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。Taiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC
官方来源
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