FDA 510(k)

内部牵开器 - 无菌

K号: K161470 · 2016-12-01

决定日期2016-12-01

产品代码MQN

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决定实质等同

器械摘要

Internal Distraction - Sterile is the device name listed in this FDA 510(k) record. The listed applicant is KLS Martin L.P.. It received FDA 510(k) clearance on 2016-12-01 under 510(k) number K161470. The device is classified under product code MQN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Internal Distraction - Sterile?

Internal Distraction - Sterile is a medical device that received FDA 510(k) clearance on 2016-12-01. The listed applicant is KLS Martin L.P.. The 510(k) number is K161470.

When did Internal Distraction - Sterile receive FDA 510(k) clearance?

Internal Distraction - Sterile received FDA 510(k) clearance on 2016-12-01, under 510(k) number K161470.

Who is the listed applicant for Internal Distraction - Sterile?

The FDA 510(k) record lists KLS Martin L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Internal Distraction - Sterile?

The FDA product code for Internal Distraction - Sterile is MQN.

列明KLS Martin L.P.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。

K260137KLS Martin IPS 口腔-Max 种植体 - MR 条件性；个体化患者解决方案 - Ti (IPS-Ti)；个体化患者解决方案 - PEEK (IPS-PEEK)；KLS Martin 个体化患者解决方案 K254162KLS Martin Ixos 系统 K253660KLS Martin Pure Pectus 系统 K250988KLS Martin Pure Pectus 系统 K250865KLS Martin IPS 前臂系统 K252573KLS Martin 颅骨植入物 - MR 条件；K944565：KLS-Martin 微型骨合成系统（1.5MM）；K971297：KLS Martin 中心驱动无钻螺丝；K060177：KLS Martin 刚性固定 - 无菌；K062570：个体化患者解决方案 - Ti (IPS-Ti)；K072707：个体化患者解决方案 - PEEK (IPS-PEEK)；K151382：个体化患者解决方案 - (IPS-PEEK) - 无菌

查看所有 33 个设备 →

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。