FDA 510(k)

PMT 面板螺钉

K号: K183589 · 2019-10-11

决定日期2019-10-11

产品代码MRW

决定实质等同

器械摘要

PMT Facet Screw 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 2019-10-11 under 510(k) number K183589. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.

常见问题

What is the PMT Facet Screw?

PMT Facet Screw is a medical device that received FDA 510(k) clearance on 2019-10-11. The listed applicant is Providence Medical Technology, Inc.. The 510(k) number is K183589.

When did PMT Facet Screw receive FDA 510(k) clearance?

PMT Facet Screw received FDA 510(k) clearance on 2019-10-11, under 510(k) number K183589.

Who is the listed applicant for PMT Facet Screw?

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 PMT Facet Screw?

The FDA product code for PMT Facet Screw 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。

K261665CORUS® 导航系统-GN K253676CORUS® 后颈椎稳定系统 3D (CORUS® PCSS 3D)K253190CORUS-LX 移植物 K251060CORUS® 导航系统-GX K251885CAVUX 骨突固定系统（CAVUX FFS）和 CORUS-LX 移植 K241035PMT 后颈椎稳定系统（PCSS）

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官方来源

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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。