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
MQV Filler, Bone Void, Calcium Compound

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQV), ordered by most recent decision date.

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Other Clearances by Bonesupport AB

K Number Device Name
K234008 CERAMENT G
K240459 Cerament Bone Void Filler
DEN210044 CERAMENT G
K201535 Cerament Bone Void Filler
K090871 CERAMENT IBONE VOID FILLER HIGH CONTRAST, MODEL A 0210-12
K051951 CERAMENT BONE VOID FILLER