FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
DEVINE SPINAL SYSTEM
K Number: K111690
·
Decision Nov 22, 2011
Classifications
1
FEI Numbers
326
Registration Numbers
326
Same Product Code
308
Applicant Total
2
Review Days
159
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Basic Information
- Device Name
- DEVINE SPINAL SYSTEM
- K Number
- K111690
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3070
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Changzhou Orthmed Medical Instrument Co., Ltd.
- Date Received
- June 16, 2011
- Decision Date
- November 22, 2011
- Product Code
- MNH
- 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 |
|---|---|---|---|
| MNH | Orthosis, Spondylolisthesis Spinal Fixation | FDA class 2 | Orthopedic |
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Other Clearances by Changzhou Orthmed Medical Instrument Co., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K101400 | LOCKING COMPRESSION PLATE | Nov 9, 2010 | Substantially Equivalent |