Trinity EVO Acetabular Shell
K-Number: K242744 · 2025-06-05
ApplicantCorin U.S.A. Limited
Decision Date2025-06-05
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Trinity EVO Acetabular Shell is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2025-06-05 under approval number K242744. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Trinity EVO Acetabular Shell?
Trinity EVO Acetabular Shell is a medical device that received FDA 510(k) clearance on 2025-06-05. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K242744.
When was Trinity EVO Acetabular Shell approved by the FDA?
Trinity EVO Acetabular Shell received FDA 510(k) clearance on 2025-06-05, under approval number K242744.
What company makes Trinity EVO Acetabular Shell?
Trinity EVO Acetabular Shell is manufactured by Corin U.S.A. Limited.
What is the FDA product code for Trinity EVO Acetabular Shell?
The FDA product code for Trinity EVO Acetabular Shell is LPH.
Related Clinical Trials
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.