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FDA 510(k)

Trinity™ Dual Mobility System

K-Number: K170359 · 2017-10-31

ApplicantCorin U.S.A. Limited
Decision Date2017-10-31
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Trinity™ Dual Mobility System is a medical device manufactured by Corin U.S.A. Limited. It received FDA 510(k) clearance on 2017-10-31 under approval number K170359. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trinity™ Dual Mobility System?

Trinity™ Dual Mobility System is a medical device that received FDA 510(k) clearance on 2017-10-31. It is manufactured by Corin U.S.A. Limited. The 510(k) number is K170359.

When was Trinity™ Dual Mobility System approved by the FDA?

Trinity™ Dual Mobility System received FDA 510(k) clearance on 2017-10-31, under approval number K170359.

What company makes Trinity™ Dual Mobility System?

Trinity™ Dual Mobility System is manufactured by Corin U.S.A. Limited.

What is the FDA product code for Trinity™ Dual Mobility System?

The FDA product code for Trinity™ Dual Mobility System is LZO.

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Other Devices by Corin U.S.A. Limited

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Related Devices (Code: LZO)

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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.

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