PRIMA 肱骨系统;PRIMA TT 肩臼
K号: K233712 · 2024-01-11
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器械摘要
常见问题
What is the PRIMA Humeral System; PRIMA TT Glenoid?
PRIMA Humeral System; PRIMA TT Glenoid is a medical device that received FDA 510(k) clearance on 2024-01-11. The listed applicant is Lima Corporate S.P.A.. The 510(k) number is K233712.
When did PRIMA Humeral System; PRIMA TT Glenoid receive FDA 510(k) clearance?
PRIMA Humeral System; PRIMA TT Glenoid received FDA 510(k) clearance on 2024-01-11, under 510(k) number K233712.
Who is the listed applicant for PRIMA Humeral System; PRIMA TT Glenoid?
The FDA 510(k) record lists Lima Corporate S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRIMA Humeral System; PRIMA TT Glenoid?
The FDA product code for PRIMA Humeral System; PRIMA TT Glenoid is MBF.
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Lima Corporate S.P.A.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:MBF)
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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