FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SMARTSET GMV GENTAMICIN BONE CEMENT
K Number: K081163
·
Decision May 14, 2008
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
18
Applicant Total
207
Review Days
20
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Basic Information
- Device Name
- SMARTSET GMV GENTAMICIN BONE CEMENT
- K Number
- K081163
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 888.3027
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- DePuy Orthopaedics, Inc.
- Date Received
- April 24, 2008
- Decision Date
- May 14, 2008
- Product Code
- MBB
- 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 |
|---|---|---|---|
| MBB | Bone Cement, Antibiotic | FDA class 2 | Orthopedic |
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