FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
GENERAL SPINAL SYSTEM
K Number: K140229
·
Decision Apr 29, 2014
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
3
Review Days
89
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Basic Information
- Device Name
- GENERAL SPINAL SYSTEM
- K Number
- K140229
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tianjin Walkman Biomaterial Co., Ltd.
- Date Received
- January 30, 2014
- Decision Date
- April 29, 2014
- Product Code
- MNI
- 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 |
|---|---|---|---|
| MNI | Orthosis, Spinal Pedicle Fixation | FDA class 2 | Orthopedic |
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