TechCare Trauma

Milvue · K242171 · 2025-01-17

TechCare Trauma is an AI-enabled medical device from Milvue, listed by FDA (510(k), K242171) with a decision date of 2025-01-17. Review panel: Radiology.

FDA submission numberK242171
Pathway510(k)
CompanyMilvue
Review panel (specialty)Radiology
FDA decision date2025-01-17
DecisionSubstantially Equivalent
Product codeQBS
ClassificationRadiological Computer Assisted Detection/Diagnosis Software For Fracture
Device class2
Regulation number892.2090
Review time (calendar days)177
Applicant countryFR

Official FDA database record · FDA AI-enabled device list

All Radiology AI devices · Full device index

Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.