FDA 510(k)
FDA class 2
Substantially Equivalent
🇸🇪 Sweden
CERAMENT BONE VOID FILLER, MODEL A0210
K Number: K073316
·
Decision Jun 20, 2008
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
7
Review Days
207
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Basic Information
- Device Name
- CERAMENT BONE VOID FILLER, MODEL A0210
- K Number
- K073316
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 888.3045
- Medical Specialty
- Orthopedic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bonesupport AB
- Date Received
- November 26, 2007
- Decision Date
- June 20, 2008
- 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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Other Clearances by Bonesupport AB
| K Number | Device Name | ||
|---|---|---|---|
| K234008 | CERAMENT G | Mar 13, 2024 | Substantially Equivalent |
| K240459 | Cerament Bone Void Filler | Mar 5, 2024 | Substantially Equivalent |
| DEN210044 | CERAMENT G | May 17, 2022 | Unknown |
| K201535 | Cerament Bone Void Filler | Oct 16, 2020 | Substantially Equivalent |
| K090871 | CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12 | Sep 4, 2009 | Substantially Equivalent |
| K051951 | CERAMENT BONE VOID FILLER | Sep 28, 2005 | Substantially Equivalent |