Medicon Epiplating System
K-Number: K241253 · 2024-12-12
ApplicantCmf Medicon Surgical, Inc.
Decision Date2024-12-12
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Medicon Epiplating System is a medical device manufactured by Cmf Medicon Surgical, Inc.. It received FDA 510(k) clearance on 2024-12-12 under approval number K241253. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Medicon Epiplating System?
Medicon Epiplating System is a medical device that received FDA 510(k) clearance on 2024-12-12. It is manufactured by Cmf Medicon Surgical, Inc.. The 510(k) number is K241253.
When was Medicon Epiplating System approved by the FDA?
Medicon Epiplating System received FDA 510(k) clearance on 2024-12-12, under approval number K241253.
What company makes Medicon Epiplating System?
Medicon Epiplating System is manufactured by Cmf Medicon Surgical, Inc..
What is the FDA product code for Medicon Epiplating System?
The FDA product code for Medicon Epiplating System is FZE.
Other Devices by Cmf Medicon Surgical, Inc.
Related Devices (Code: FZE)
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.