FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Seneka I Polyscrew Pedicle Fixation System
K Number: K151849
·
Decision Sep 30, 2015
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
2
Review Days
85
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Basic Information
- Device Name
- Seneka I Polyscrew Pedicle Fixation System
- K Number
- K151849
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Senecka Spine
- Date Received
- July 7, 2015
- Decision Date
- September 30, 2015
- 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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Other Clearances by Senecka Spine
| K Number | Device Name | ||
|---|---|---|---|
| K153525 | Seneka II Polyscrew Pedicle Fixation System | Jan 28, 2016 | Substantially Equivalent |