Cleared Traditional

MedicloseTM System

K213271 · Health Value Creation B.V., Trading AS Corporis Medical · General & Plastic Surgery
Aug 2023
Decision
700d
Days
Class 2
Risk

About This 510(k) Submission

K213271 is an FDA 510(k) clearance for the MedicloseTM System, a Endoscopic Tissue Approximation Device (Class II — Special Controls, product code OCW), submitted by Health Value Creation B.V., Trading AS Corporis Medical (Maastricht, NL). The FDA issued a Cleared decision on August 31, 2023, 700 days after receiving the submission on September 30, 2021. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K213271 FDA.gov
FDA Decision Cleared SESE
Date Received September 30, 2021
Decision Date August 31, 2023
Days to Decision 700 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OCW — Endoscopic Tissue Approximation Device
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Aid In Endoscopically Placing Sutures, Staples, Clips, And Other Fastening Tools Through Tissue.

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