FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
K7C SPACER
K Number: K123388
·
Decision Jan 4, 2013
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
3
Review Days
63
Basic Information
- Device Name
- K7C SPACER
- K Number
- K123388
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3080
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- K7, LLC
- Date Received
- November 2, 2012
- Decision Date
- January 4, 2013
- Product Code
- ODP
- 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 |
|---|---|---|---|
| ODP | Intervertebral Fusion Device With Bone Graft, Cervical | FDA class 2 | Orthopedic |
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