Trinity PLUS Acetabular Shell
K-Number: K172551 · 2018-06-15
ApplicantCorin U.S.A. Limited
Decision Date2018-06-15
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Trinity PLUS Acetabular Shell is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2018-06-15 under approval number K172551. 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 PLUS Acetabular Shell?
Trinity PLUS Acetabular Shell is a medical device that received FDA 510(k) clearance on 2018-06-15. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K172551.
When was Trinity PLUS Acetabular Shell approved by the FDA?
Trinity PLUS Acetabular Shell received FDA 510(k) clearance on 2018-06-15, under approval number K172551.
What company makes Trinity PLUS Acetabular Shell?
Trinity PLUS Acetabular Shell is manufactured by Corin U.S.A. Limited.
What is the FDA product code for Trinity PLUS Acetabular Shell?
The FDA product code for Trinity PLUS 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.