FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇮 Finland

INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE

K Number: K090177 · Decision Feb 20, 2009
Classifications
1
FEI Numbers
229
Registration Numbers
229
Same Product Code
491
Applicant Total
14
Review Days
28

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Basic Information

Device Name
INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE
K Number
K090177
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3045
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Inion OY
Date Received
January 23, 2009
Decision Date
February 20, 2009
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 Inion OY

K Number Device Name
K251441 Inion CPS 1.5 Baby Bioabsorbable Fixation System; Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System
K251472 Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System; Inion CPS 1.5 Baby Bioabsorbable Fixation System
K203105 Inion CompressOn Screw
K191764 Inion BioRestore
K151360 Inion Spinal Graft Containment System
K133932 INION FREEDOMPIN
K123672 INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FREEDOMSCREW)
K122890 INION CPS ORBITAL PLATES
K070998 INION BIORESTORE
K071464 INION HEXALON BIODEGRADABLE ACL/PCL SCREW
Search all 14 clearances from Inion OY →