手术预览
K号: K171534 · 2017-11-08
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器械摘要
SurgicalPreview is the device name listed in this FDA 510(k) record. The listed applicant is Endo Vantage, LLC. It received FDA 510(k) clearance on 2017-11-08 under 510(k) number K171534. The device is classified under product code PZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SurgicalPreview?
SurgicalPreview is a medical device that received FDA 510(k) clearance on 2017-11-08. The listed applicant is Endo Vantage, LLC. The 510(k) number is K171534.
When did SurgicalPreview receive FDA 510(k) clearance?
SurgicalPreview received FDA 510(k) clearance on 2017-11-08, under 510(k) number K171534.
Who is the listed applicant for SurgicalPreview?
The FDA 510(k) record lists Endo Vantage, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurgicalPreview?
The FDA product code for SurgicalPreview is PZO.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：PZO）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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