FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
C-CURVE Interbody Fusion Device
K Number: K210470
·
Decision Sep 3, 2021
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
25
Review Days
198
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Basic Information
- Device Name
- C-CURVE Interbody Fusion Device
- K Number
- K210470
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medicrea International SA
- Date Received
- February 17, 2021
- Decision Date
- September 3, 2021
- Product Code
- OVE
- 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 |
|---|---|---|---|
| OVE | Intervertebral Fusion Device With Integrated Fixation, Cervical | FDA class 2 | Orthopedic |
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