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FDA 510(k)

EVOS Patella Plates

K-Number: K240487 · 2024-09-03

ApplicantSmith & Nephew
Decision Date2024-09-03
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EVOS Patella Plates is a medical device manufactured by Smith & Nephew. It received FDA 510(k) clearance on 2024-09-03 under approval number K240487. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVOS Patella Plates?

EVOS Patella Plates is a medical device that received FDA 510(k) clearance on 2024-09-03. It is manufactured by Smith & Nephew. The 510(k) number is K240487.

When was EVOS Patella Plates approved by the FDA?

EVOS Patella Plates received FDA 510(k) clearance on 2024-09-03, under approval number K240487.

What company makes EVOS Patella Plates?

EVOS Patella Plates is manufactured by Smith & Nephew.

What is the FDA product code for EVOS Patella Plates?

The FDA product code for EVOS Patella Plates is HRS.

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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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