EVOS Small Fragment Lower Extremity Plates
K-Number: K170457 · 2017-06-14
Device Summary
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. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K170457.
When did EVOS Small Fragment Lower Extremity Plates receive FDA 510(k) clearance?
EVOS Small Fragment Lower Extremity Plates received FDA 510(k) clearance on 2017-06-14, under 510(k) number K170457.
Who is the listed applicant for EVOS Small Fragment Lower Extremity Plates?
The FDA 510(k) record lists Smith & Nephew, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Smith & Nephew, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: HRS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.