Alloclassic Zweymuller SL股骨柄,Alloclassic Zweymuller SL偏移股骨柄
K号: K193050 · 2019-12-26
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器械摘要
常见问题
What is the Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem?
Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem is a medical device that received FDA 510(k) clearance on 2019-12-26. The listed applicant is Zimmer GmbH. The 510(k) number is K193050.
When did Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem receive FDA 510(k) clearance?
Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem received FDA 510(k) clearance on 2019-12-26, under 510(k) number K193050.
Who is the listed applicant for Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem?
The FDA 510(k) record lists Zimmer GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem?
The FDA product code for Alloclassic Zweymuller SL Femoral Stem, Alloclassic Zweymuller SL Offset Femoral Stem is LZO.
相关临床试验
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列明Zimmer GmbH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:LZO)
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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