FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

Axial3D Cloud Segmentation Service

K Number: K221511 · Decision Jun 23, 2022
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
4
Review Days
30

Basic Information

Device Name
Axial3D Cloud Segmentation Service
K Number
K221511
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Axial Medical Printing Limited
Date Received
May 24, 2022
Decision Date
June 23, 2022
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

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Other Clearances by Axial Medical Printing Limited

K Number Device Name
K231607 Axial3D Cloud Segmentation Service
K232841 Axial3D Insight
K222745 Axial3D Insight