FDA 510(k)
FDA class 2
Substantially Equivalent
🇮🇹 Italy
OrthoNext Platform System
K Number: K202519
·
Decision Oct 27, 2020
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
16
Review Days
56
Basic Information
- Device Name
- OrthoNext Platform System
- K Number
- K202519
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.2050
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Orthofix Srl
- Date Received
- September 1, 2020
- Decision Date
- October 27, 2020
- Product Code
- LLZ
- 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 |
|---|---|---|---|
| LLZ | System, Image Processing, Radiological | FDA class 2 | Radiology |
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