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FDA 510(k)

VERSAFITCUP CC TRIO

K-Number: K103352 · 2011-02-11

ApplicantMedacta International
Decision Date2011-02-11
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VERSAFITCUP CC TRIO is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International. It received FDA 510(k) clearance on 2011-02-11 under 510(k) number K103352. 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 VERSAFITCUP CC TRIO?

VERSAFITCUP CC TRIO is a medical device that received FDA 510(k) clearance on 2011-02-11. The listed applicant is Medacta International. The 510(k) number is K103352.

When did VERSAFITCUP CC TRIO receive FDA 510(k) clearance?

VERSAFITCUP CC TRIO received FDA 510(k) clearance on 2011-02-11, under 510(k) number K103352.

Who is the listed applicant for VERSAFITCUP CC TRIO?

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

What is the FDA product code for VERSAFITCUP CC TRIO?

The FDA product code for VERSAFITCUP CC TRIO 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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