Medline ReNewal Reprocessed 斯特林克 外固定装置
K号: K163028 · 2016-12-28
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器械摘要
常见问题
What is the Medline ReNewal Reprocessed Stryker External Fixation Devices?
Medline ReNewal Reprocessed Stryker External Fixation Devices is a medical device that received FDA 510(k) clearance on 2016-12-28. The listed applicant is Surgical Instrument Service and Savings, Inc.. The 510(k) number is K163028.
When did Medline ReNewal Reprocessed Stryker External Fixation Devices receive FDA 510(k) clearance?
Medline ReNewal Reprocessed Stryker External Fixation Devices received FDA 510(k) clearance on 2016-12-28, under 510(k) number K163028.
Who is the listed applicant for Medline ReNewal Reprocessed Stryker External Fixation Devices?
The FDA 510(k) record lists Surgical Instrument Service and Savings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medline ReNewal Reprocessed Stryker External Fixation Devices?
The FDA product code for Medline ReNewal Reprocessed Stryker External Fixation Devices is JEC.
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列明Surgical Instrument Service and Savings, 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。
相关器械(代码:JEC)
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
在 FDA 数据库中查看 →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。
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