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FDA 510(k)

CORIN TRINITY-I ACETABULAR SHELL

K-Number: K122305 · 2012-11-21

ApplicantCorin USA
Decision Date2012-11-21
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN TRINITY-I ACETABULAR SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2012-11-21 under 510(k) number K122305. 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 CORIN TRINITY-I ACETABULAR SHELL?

CORIN TRINITY-I ACETABULAR SHELL is a medical device that received FDA 510(k) clearance on 2012-11-21. The listed applicant is Corin USA. The 510(k) number is K122305.

When did CORIN TRINITY-I ACETABULAR SHELL receive FDA 510(k) clearance?

CORIN TRINITY-I ACETABULAR SHELL received FDA 510(k) clearance on 2012-11-21, under 510(k) number K122305.

Who is the listed applicant for CORIN TRINITY-I ACETABULAR SHELL?

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

What is the FDA product code for CORIN TRINITY-I ACETABULAR SHELL?

The FDA product code for CORIN TRINITY-I ACETABULAR SHELL is 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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