FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ORTHROS POSTERIOR STABILIZATION SYSTEM
K Number: K133366
·
Decision Apr 8, 2014
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
4
Review Days
158
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Basic Information
- Device Name
- ORTHROS POSTERIOR STABILIZATION SYSTEM
- K Number
- K133366
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Camber Spine
- Date Received
- November 1, 2013
- Decision Date
- April 8, 2014
- 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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