FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO S4 SPINAL SYSTEM
K Number: K062327
·
Decision Mar 14, 2007
Classifications
1
FEI Numbers
413
Registration Numbers
413
Same Product Code
873
Applicant Total
174
Review Days
216
Basic Information
- Device Name
- MODIFICATION TO S4 SPINAL SYSTEM
- K Number
- K062327
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- AESCULAP, INC.
- Date Received
- August 10, 2006
- Decision Date
- March 14, 2007
- 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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