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FDA 510(k)

TRINITY ACETABULAR SYSTEM

K-Number: K130128 · 2013-03-08

ApplicantCorin Medical
Decision Date2013-03-08
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRINITY ACETABULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Corin Medical. It received FDA 510(k) clearance on 2013-03-08 under 510(k) number K130128. 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 ACETABULAR SYSTEM?

TRINITY ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 2013-03-08. The listed applicant is Corin Medical. The 510(k) number is K130128.

When did TRINITY ACETABULAR SYSTEM receive FDA 510(k) clearance?

TRINITY ACETABULAR SYSTEM received FDA 510(k) clearance on 2013-03-08, under 510(k) number K130128.

Who is the listed applicant for TRINITY ACETABULAR SYSTEM?

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

What is the FDA product code for TRINITY ACETABULAR SYSTEM?

The FDA product code for TRINITY ACETABULAR SYSTEM 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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