FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇭 Switzerland
SPINEART Navigation Instrument System
K Number: K210472
·
Decision Mar 19, 2021
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
44
Review Days
30
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Basic Information
- Device Name
- SPINEART Navigation Instrument System
- K Number
- K210472
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 882.4560
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Spineart
- Date Received
- February 17, 2021
- Decision Date
- March 19, 2021
- Product Code
- OLO
- Advisory Committee
- Neurology
- 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 |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | FDA class 2 | Neurology |
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