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

CORIOGRAPH Pre-Op Planning and Modeling Services

K Number: K250921 · Decision Jun 25, 2025
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
26
Applicant Total
22
Review Days
90

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Basic Information

Device Name
CORIOGRAPH Pre-Op Planning and Modeling Services
K Number
K250921
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Blue Belt Technologies, Inc.
Date Received
March 27, 2025
Decision Date
June 25, 2025
Product Code
PBF
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
PBF Orthopaedic Surgical Planning And Instrument Guides

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Other Clearances by Blue Belt Technologies, Inc.

K Number Device Name
K260601 REAL INTELLIGENCE™ CORI™
K252841 REAL INTELLIGENCE™ CORI™ XT (CORI XT)
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
K212040 RI.HIP MODELER
K212537 REAL INTELLIGENCE CORI (CORI)
Search all 22 clearances from Blue Belt Technologies, Inc. →