膝关节+
K号: K202750 · 2021-04-21
广告
决定日期2021-04-21
产品代码SBF
咨询委员会NE
请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同
器械摘要
Knee+ is the device name listed in this FDA 510(k) record. The listed applicant is Pixee Medical. It received FDA 510(k) clearance on 2021-04-21 under 510(k) number K202750. The device is classified under product code SBF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Knee+?
Knee+ is a medical device that received FDA 510(k) clearance on 2021-04-21. The listed applicant is Pixee Medical. The 510(k) number is K202750.
When did Knee+ receive FDA 510(k) clearance?
Knee+ received FDA 510(k) clearance on 2021-04-21, under 510(k) number K202750.
Who is the listed applicant for Knee+?
The FDA 510(k) record lists Pixee Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Knee+?
The FDA product code for Knee+ is SBF.
列明Pixee Medical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：SBF）
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。
广告