FDA 510(k)

ApolloHipX（THR.SS.0001）

K号: K241808 · 2025-01-07

决定日期2025-01-07

产品代码LLZ

咨询委员会RA

决定实质等同

器械摘要

ApolloHipX (THR.SS.0001) is the device name listed in this FDA 510(k) record. The listed applicant is Corin U.S.A. Limited. It received FDA 510(k) clearance on 2025-01-07 under 510(k) number K241808. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ApolloHipX (THR.SS.0001)?

ApolloHipX (THR.SS.0001) is a medical device that received FDA 510(k) clearance on 2025-01-07. The listed applicant is Corin U.S.A. Limited. The 510(k) number is K241808.

When did ApolloHipX (THR.SS.0001) receive FDA 510(k) clearance?

ApolloHipX (THR.SS.0001) received FDA 510(k) clearance on 2025-01-07, under 510(k) number K241808.

Who is the listed applicant for ApolloHipX (THR.SS.0001)?

The FDA 510(k) record lists Corin U.S.A. Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ApolloHipX (THR.SS.0001)?

The FDA product code for ApolloHipX (THR.SS.0001) is LLZ.

列明Corin U.S.A. Limited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。

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