FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Orthoscan TAU MVP Mini C-Arm System
K Number: K252579
·
Decision Jan 14, 2026
Classifications
1
FEI Numbers
68
Registration Numbers
68
Same Product Code
81
Applicant Total
3
Review Days
152
Basic Information
- Device Name
- Orthoscan TAU MVP Mini C-Arm System
- K Number
- K252579
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1650
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ziehm-Orthoscan, Inc.
- Date Received
- August 15, 2025
- Decision Date
- January 14, 2026
- Product Code
- OXO
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| OXO | Image-Intensified Fluoroscopic X-Ray System, Mobile | FDA class 2 | Radiology |
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