Legion Cone System
K-Number: K162775 · 2017-01-13
Device Summary
Frequently Asked Questions
What is the Legion Cone System?
Legion Cone System is a medical device that received FDA 510(k) clearance on 2017-01-13. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K162775.
When did Legion Cone System receive FDA 510(k) clearance?
Legion Cone System received FDA 510(k) clearance on 2017-01-13, under 510(k) number K162775.
Who is the listed applicant for Legion Cone System?
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 Legion Cone System?
The FDA product code for Legion Cone System is JWH.
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: JWH)
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.