EVOS Patella Plates
K-Number: K240487 · 2024-09-03
Device Summary
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. The listed applicant is Smith & Nephew. The 510(k) number is K240487.
When did EVOS Patella Plates receive FDA 510(k) clearance?
EVOS Patella Plates received FDA 510(k) clearance on 2024-09-03, under 510(k) number K240487.
Who is the listed applicant for EVOS Patella Plates?
The FDA 510(k) record lists Smith & Nephew as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EVOS Patella Plates?
The FDA product code for EVOS Patella 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 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.