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
34
Registration Numbers
34
Same Product Code
21
Applicant Total
15
Review Days
90

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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K Number Device Name
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K201022 REAL INTELLIGENCE CORI (CORI)
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