510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K260322Substantially Equivalent

Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX)

Mighty Oak Medical, Englewood CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260322 is the FDA 510(k) clearance record for Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX), a class II device, cleared for Mighty Oak Medical on under FDA product code QIH (Automated Radiological Image Processing Software). FDA's definition for product code QIH reads: "To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the...". FDA records list 10 510(k) clearances for Mighty Oak Medical, from to . As of , FDA records show no recalls naming K260322.

Clearance record

Decision date
Received
(132 days to decision)
Product code
QIH Automated Radiological Image Processing Software
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Mighty Oak Medical 750 W. Hampden Ave., Englewood CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QIH

Trailing 12 months
87 clearances under product code QIH in the twelve months to October 2026, June 2026 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code QIH, trailing twelve months
MonthClearances
November 20253
December 202510
January 20265
February 20264
March 20268
April 202610
May 202610
June 202611
July 20269
August 20268
September 20269
October 20260