510(k) K231607

Axial3D Cloud Segmentation Service by Axial Medical Printing Limited — Product Code LLZ

K231607 is an FDA 510(k) premarket notification submitted by Axial Medical Printing Limited for the device "Axial3D Cloud Segmentation Service". The FDA issued a decision of Substantially Equivalent on January 24, 2024. The device falls under product code LLZ (System, Image Processing, Radiological), a Class II device regulated under 21 CFR 892.2050. Axial Medical Printing Limited has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 2024
Date Received
June 1, 2023
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type