Persona 定制膝关节系统 (Persona Porous Plasma Spray PPS Femurs)
K号: K253189 · 2026-03-09
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器械摘要
常见问题
What is the Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?
Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is Zimmer, Inc.. The 510(k) number is K253189.
When did Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) receive FDA 510(k) clearance?
Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) received FDA 510(k) clearance on 2026-03-09, under 510(k) number K253189.
Who is the listed applicant for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?
FDA 510(k)记录显示Zimmer, Inc.为申请人。这本身并不能确立该设备的制造商。
What is the FDA product code for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)?
The FDA product code for Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs) is MBH.
相关临床试验
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。
列明Zimmer, 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:MBH)
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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