FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RI.HIP MODELER

K Number: K212040 · Decision Mar 11, 2022
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
15
Review Days
254

Basic Information

Device Name
RI.HIP MODELER
K Number
K212040
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Blue Belt Technologies, Inc.
Date Received
June 30, 2021
Decision Date
March 11, 2022
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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.

View all

Other Clearances by Blue Belt Technologies, Inc.

K Number Device Name
K250921 CORIOGRAPH Pre-Op Planning and Modeling Services
K242272 CORIOGRAPH Pre-Op Planning and Modeling Services
K240139 Real Intelligence™ CORI™
K231963 REAL INTELLIGENCE™ CORI™
K221224 REAL INTELLIGENCE CORI
K220958 Real Intelligence Cori
K220255 REAL INTELLIGENCE CORI
K212537 REAL INTELLIGENCE CORI (CORI)
K201022 REAL INTELLIGENCE CORI (CORI)
K193120 Real Intelligence Cori
Search all 15 clearances from Blue Belt Technologies, Inc. →