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FDA 510(k)

EVOS Small Fragment Lower Extremity Plates

K-Number: K170457 · 2017-06-14

ApplicantSmith & Nephew, Inc.
Decision Date2017-06-14
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EVOS Small Fragment Lower Extremity Plates is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2017-06-14 under approval number K170457. 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 Small Fragment Lower Extremity Plates?

EVOS Small Fragment Lower Extremity Plates is a medical device that received FDA 510(k) clearance on 2017-06-14. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K170457.

When was EVOS Small Fragment Lower Extremity Plates approved by the FDA?

EVOS Small Fragment Lower Extremity Plates received FDA 510(k) clearance on 2017-06-14, under approval number K170457.

What company makes EVOS Small Fragment Lower Extremity Plates?

EVOS Small Fragment Lower Extremity Plates is manufactured by Smith & Nephew, Inc..

What is the FDA product code for EVOS Small Fragment Lower Extremity Plates?

The FDA product code for EVOS Small Fragment Lower Extremity Plates is HRS.

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Related PubMed Literature

PMID: 41638310 Lower Extremity Complications in Adults With Type 2 Diabetes Treated With Glucagon-Like Peptide-1 Receptor Agonists, Sodium-Glucose Cotransporter 2 Inhibitors, Dipeptidyl Peptidase-4 Inhibitors, and Sulfonylureas: An Emulated Target Trial. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists (2026)

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Related Devices (Code: 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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