FDA 510(k)

Medicon Epiplating System

K-Number: K241253 · 2024-12-12

Decision Date2024-12-12

Product CodeFZE

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Medicon Epiplating System is the device name listed in this FDA 510(k) record. The listed applicant is Cmf Medicon Surgical, Inc.. It received FDA 510(k) clearance on 2024-12-12 under 510(k) 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. The listed applicant is Cmf Medicon Surgical, Inc.. The 510(k) number is K241253.

When did Medicon Epiplating System receive FDA 510(k) clearance?

Medicon Epiplating System received FDA 510(k) clearance on 2024-12-12, under 510(k) number K241253.

Who is the listed applicant for Medicon Epiplating System?

The FDA 510(k) record lists Cmf Medicon Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medicon Epiplating System?

The FDA product code for Medicon Epiplating System is FZE.

Other records listing Cmf Medicon Surgical, 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.