Cleared Traditional

K233458 - CM005 Standard (CM005) (FDA 510(k) Clearance)

Also includes:
CM004 Mini (CM004)
Jul 2024
Decision
266d
Days
Class 2
Risk

K233458 is an FDA 510(k) clearance for the CM005 Standard (CM005). This device is classified as a Tissue Adhesive For The Topical Approximation Of Skin (Class II - Special Controls, product code MPN).

Submitted by Connexicon Medical , Ltd. (Dublin, IE). The FDA issued a Cleared decision on July 15, 2024, 266 days after receiving the submission on October 23, 2023.

This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4010. Docket Number: 2006p-0071 - May 5, 2008 - Reclassified From Class 3 Pma To Class 2 510(k)..

Submission Details

510(k) Number K233458 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 2023
Decision Date July 15, 2024
Days to Decision 266 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code MPN - Tissue Adhesive For The Topical Approximation Of Skin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 878.4010
Definition Docket Number: 2006p-0071 - May 5, 2008 - Reclassified From Class 3 Pma To Class 2 510(k).