关节，颞下颌关节，植入物
PMA编号：P980052 · 2026-03-06
广告
决定日期2026-03-06
PMA 编号P980052
产品代码LZD
设备分类第3类
医疗专科D
法规编号21 CFR 8
咨询委员会DE
请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。
器械摘要
Joint, temporomandibular, implant is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger, GmbH & Co KG. It received FDA 510(k) clearance on 2026-03-06. The device is classified under product code LZD. It was reviewed by the DE advisory panel.
常见问题
What is the Joint, temporomandibular, implant?
Joint, temporomandibular, implant is a medical device that received FDA 510(k) clearance on 2026-03-06. The listed applicant is Stryker Leibinger, GmbH & Co KG.
When did Joint, temporomandibular, implant receive FDA 510(k) clearance?
The clearance date for Joint, temporomandibular, implant can be found in the official FDA records.
Who is the listed applicant for Joint, temporomandibular, implant?
The FDA 510(k) record lists Stryker Leibinger, GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Joint, temporomandibular, implant?
The FDA product code for Joint, temporomandibular, implant is LZD.
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