Legion Cone System
K-Number: K162775 · 2017-01-13
ApplicantSmith & Nephew, Inc.
Decision Date2017-01-13
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Legion Cone System is a medical device manufactured by Smith & Nephew, Inc.. It received FDA 510(k) clearance on 2017-01-13 under approval number K162775. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Smith & Nephew, Inc.. The 510(k) number is K162775.
When was Legion Cone System approved by the FDA?
Legion Cone System received FDA 510(k) clearance on 2017-01-13, under approval number K162775.
What company makes Legion Cone System?
Legion Cone System is manufactured by Smith & Nephew, Inc..
What is the FDA product code for Legion Cone System?
The FDA product code for Legion Cone System is JWH.
Related Clinical Trials
Other Devices by Smith & Nephew, Inc.
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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.