FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
JAZZ Spinal System
K Number: K240392
·
Decision May 6, 2024
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
3
Review Days
88
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Basic Information
- Device Name
- JAZZ Spinal System
- K Number
- K240392
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Implanet
- Date Received
- February 8, 2024
- Decision Date
- May 6, 2024
- Product Code
- NKB
- 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 |
|---|---|---|---|
| NKB | Thoracolumbosacral Pedicle Screw System | FDA class 2 | Orthopedic |
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