FDA 510(k)

ApolloHipX (THR.SS.0001)

K-Number: K241808 · 2025-01-07

Decision Date2025-01-07

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K241808.

When was ApolloHipX (THR.SS.0001) approved by the FDA?

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

What company makes ApolloHipX (THR.SS.0001)?

ApolloHipX (THR.SS.0001) is manufactured by Corin U.S.A. Limited.

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

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

Other Devices by Corin U.S.A. Limited

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.