Tritanium® PL Cage
K号: K160955 · 2016-07-21
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器械摘要
Tritanium® PL Cage is the device name listed in this FDA 510(k) record. The listed applicant is Stryker. It received FDA 510(k) clearance on 2016-07-21 under 510(k) number K160955. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Tritanium® PL Cage?
Tritanium® PL Cage is a medical device that received FDA 510(k) clearance on 2016-07-21. The listed applicant is Stryker. The 510(k) number is K160955.
When did Tritanium® PL Cage receive FDA 510(k) clearance?
Tritanium® PL Cage received FDA 510(k) clearance on 2016-07-21, under 510(k) number K160955.
Who is the listed applicant for Tritanium® PL Cage?
The FDA 510(k) record lists Stryker as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tritanium® PL Cage?
The FDA product code for Tritanium® PL Cage is MAX.
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相关器械（代码：MAX）
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
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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