510(k) K260322

Device
Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)
Applicant
Mighty Oak Medical
510(k) number
K260322
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2026-06-11
Date received
2026-01-30
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Mark Wylie
Address
750 W. Hampden Ave. Suite 120 Englewood CO US 80110 80110

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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