FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MedCAD® AccuStride System
K Number: K251709
·
Decision Nov 4, 2025
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
26
Applicant Total
9
Review Days
154
Basic Information
- Device Name
- MedCAD® AccuStride System
- K Number
- K251709
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3030
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medcad
- Date Received
- June 3, 2025
- Decision Date
- November 4, 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 Medcad
| K Number | Device Name | ||
|---|---|---|---|
| K252064 | MedCAD® AccuStride System | Mar 27, 2026 | Substantially Equivalent |
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| K230398 | MedCAD® AccuPlate® 3DTi Patient-Specific Plating System | Sep 26, 2023 | Substantially Equivalent |
| K223421 | MedCAD AccuPlan Orthopedics System | Sep 20, 2023 | Substantially Equivalent |
| K223024 | MedCAD AccuPlan System | Mar 7, 2023 | Substantially Equivalent |
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| K192282 | MedCAD® AccuPlan® System | Oct 29, 2020 | Substantially Equivalent |