FDA 510(k)

Alphatec 导航仪器

K号: K153603 · 2016-04-29

决定日期2016-04-29

产品代码OLO

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决定实质等同

器械摘要

Alphatec Navigation Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec Spine, Inc.. It received FDA 510(k) clearance on 2016-04-29 under 510(k) number K153603. 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 Alphatec Navigation Instruments?

Alphatec Navigation Instruments is a medical device that received FDA 510(k) clearance on 2016-04-29. The listed applicant is Alphatec Spine, Inc.. The 510(k) number is K153603.

When did Alphatec Navigation Instruments receive FDA 510(k) clearance?

Alphatec Navigation Instruments received FDA 510(k) clearance on 2016-04-29, under 510(k) number K153603.

Who is the listed applicant for Alphatec Navigation Instruments?

FDA 510(k)记录将Alphatec Spine, Inc.列为申请人。这本身并不足以确立该设备制造商的身份。

What is the FDA product code for Alphatec Navigation Instruments?

The FDA product code for Alphatec Navigation Instruments is OLO.

列明Alphatec Spine, Inc.为申报人的其他记录

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。

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