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 | Device Class | Medical Specialty |
|---|---|---|---|
| PBF | Orthopaedic Surgical Planning And Instrument Guides | FDA class 2 | Orthopedic |
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Other Clearances by Blue Belt Technologies, Inc.
| K Number | Device Name | ||
|---|---|---|---|
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| K220255 | REAL INTELLIGENCE CORI | Mar 29, 2022 | Substantially Equivalent |
| K212040 | RI.HIP MODELER | Mar 11, 2022 | Substantially Equivalent |
| K212537 | REAL INTELLIGENCE CORI (CORI) | Nov 3, 2021 | Substantially Equivalent |
| K201022 | REAL INTELLIGENCE CORI (CORI) | Jun 12, 2020 | Substantially Equivalent |
| K193120 | Real Intelligence Cori | Feb 14, 2020 | Substantially Equivalent |