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FDA 510(k)

Anatase 脊柱手术导航系统,型号:SNS-Spine2-S和SNS-spine2-V

K号: K220348 · 2022-07-14

决定日期2022-07-14
产品代码OLO
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决定实质等同

器械摘要

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is the device name listed in this FDA 510(k) record. The listed applicant is Remex Medical Corporation. It received FDA 510(k) clearance on 2022-07-14 under 510(k) number K220348. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is a medical device that received FDA 510(k) clearance on 2022-07-14. The listed applicant is Remex Medical Corporation. The 510(k) number is K220348.

When did Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V receive FDA 510(k) clearance?

Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V received FDA 510(k) clearance on 2022-07-14, under 510(k) number K220348.

Who is the listed applicant for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

The FDA 510(k) record lists Remex Medical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V?

The FDA product code for Anatase Spine Surgery Navigation System, Model number: SNS-Spine2-S and SNS-spine2-V is OLO.

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:OLO)

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

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