510(k) K261641

Device
Lower Limb AI (LLAI)
Applicant
AI Planning Logic, Inc.
510(k) number
K261641
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2026-08-18
Date received
2026-05-18
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
Philippe Ballaire
Address
1617 Ronne Dr. Santa Rosa CA US 95404 95404

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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