CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12
FDA 510(k) clearance K090871 · decided 2009-09-04
Clearance details
- K-number
- K090871
- Device name
- CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12
- Applicant
- Bonesupport AB
- Decision
- Substantially Equivalent
- Date received
- 2009-03-30
- Decision date
- 2009-09-04
- Days to decision
- 158 days
- Clearance type
- Traditional
- Product code
- MQV
- Device class
- 2
- Regulation number
- 888.3045
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Lund, SE
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.