Cleared Traditional

K212915 - MVision AI Segmentation (FDA 510(k) Clearance)

May 2022
Decision
232d
Days
Class 2
Risk

K212915 is an FDA 510(k) clearance for the MVision AI Segmentation. This device is classified as a Radiological Image Processing Software For Radiation Therapy (Class II - Special Controls, product code QKB).

Submitted by MVision AI (Helsinki, FI). The FDA issued a Cleared decision on May 3, 2022, 232 days after receiving the submission on September 13, 2021.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050. To Provide Semi-automatic Or Fully-automated Radiological Image Processing And Analysis Tools For Radiation Therapy. Software Implementing Artificial Intelligence (ai) Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Radiological Images. In These Devices, The Algorithm Training Images Typically Impact Device Performance. Ai Based Radiological Image Processing Software Is Intended To Be Used In The Workflow Of Radiation Therapy. Adaptive Ai Algorithms Are Not Within The Scope Of This Product Code. Primary Radiation Dose Calculation Or Plan Optimization For Treatment Planning Are Not Within Scope Of This Product Code..

Submission Details

510(k) Number K212915 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 13, 2021
Decision Date May 03, 2022
Days to Decision 232 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code QKB - Radiological Image Processing Software For Radiation Therapy
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050
Definition To Provide Semi-automatic Or Fully-automated Radiological Image Processing And Analysis Tools For Radiation Therapy. Software Implementing Artificial Intelligence (ai) Including Nonadaptive Machine Learning Algorithms Trained With Clinical And/or Artificial Radiological Images. In These Devices, The Algorithm Training Images Typically Impact Device Performance. Ai Based Radiological Image Processing Software Is Intended To Be Used In The Workflow Of Radiation Therapy. Adaptive Ai Algorithms Are Not Within The Scope Of This Product Code. Primary Radiation Dose Calculation Or Plan Optimization For Treatment Planning Are Not Within Scope Of This Product Code.