假肢，髌股胫骨，半限制型，金属/聚合物，活动轴承
PMA编号：P060037 · 2026-09-24
广告
器械摘要
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code NJL. It was reviewed by the OR advisory panel.
常见问题
What is the Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Zimmer, Inc..
When did Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing receive FDA 510(k) clearance?
The clearance date for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing can be found in the official FDA records.
Who is the listed applicant for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing?
The FDA product code for Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing is NJL.
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。
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