FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
JAX
K Number: K010555
·
Decision Feb 25, 2003
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
529
Review Days
729
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Basic Information
- Device Name
- JAX
- K Number
- K010555
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3045
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Smith & Nephew, Inc.
- Date Received
- February 26, 2001
- Decision Date
- February 25, 2003
- Product Code
- MQV
- 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 |
|---|---|---|---|
| MQV | Filler, Bone Void, Calcium Compound | FDA class 2 | Orthopedic |
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