FDA 510(k)

ALLY®椎间孔螺钉

K号: K163374 · 2017-02-16

决定日期2017-02-16

产品代码MRW

决定实质等同

器械摘要

ALLY™ Facet Screws is the device name listed in this FDA 510(k) record. The listed applicant is Providence Medical Technology, Inc.. It received FDA 510(k) clearance on 2017-02-16 under 510(k) number K163374. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

常见问题

What is the ALLY™ Facet Screws?

ALLY™ Facet Screws is a medical device that received FDA 510(k) clearance on 2017-02-16. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K163374.

When did ALLY™ Facet Screws receive FDA 510(k) clearance?

ALLY™ Facet Screws received FDA 510(k) clearance on 2017-02-16, under 510(k) number K163374.

Who is the listed applicant for ALLY™ Facet Screws?

The FDA 510(k) record lists Providence Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLY™ Facet Screws?

The FDA product code for ALLY™ Facet Screws is MRW.

列明Providence Medical Technology, 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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官方来源

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