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FDA 510(k)

VerSys Cemented Revision/Calcar

K-Number: K210842 · 2021-12-10

ApplicantZimmer, Inc.
Decision Date2021-12-10
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VerSys Cemented Revision/Calcar is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2021-12-10 under approval number K210842. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VerSys Cemented Revision/Calcar?

VerSys Cemented Revision/Calcar is a medical device that received FDA 510(k) clearance on 2021-12-10. It is manufactured by Zimmer, Inc.. The 510(k) number is K210842.

When was VerSys Cemented Revision/Calcar approved by the FDA?

VerSys Cemented Revision/Calcar received FDA 510(k) clearance on 2021-12-10, under approval number K210842.

What company makes VerSys Cemented Revision/Calcar?

VerSys Cemented Revision/Calcar is manufactured by Zimmer, Inc..

What is the FDA product code for VerSys Cemented Revision/Calcar?

The FDA product code for VerSys Cemented Revision/Calcar is JDI.

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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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